Transcript #00004951 (NM_014246.1, CELSR1 gene)

Transcript name cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila)
Gene name CELSR1 (cadherin, EGF LAG seven-pass G-type receptor 1 (flamingo homolog, Drosophila))
Chromosome 22
Transcript - NCBI ID NM_014246.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_055061.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

162 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-/. - c.18_20del r.(?) p.(Pro7del)
-/. - c.137C>T r.(?) p.(Pro46Leu)
?/. - c.137C>T r.(?) p.(Pro46Leu)
?/. - c.158G>T r.(?) p.(Gly53Val)
-?/. - c.270C>A r.(?) p.(Val90=)
-/. - c.280G>A r.(?) p.(Ala94Thr)
-/. - c.291C>G r.(?) p.(=)
-/. - c.408C>T r.(?) p.(Pro136=)
-?/. - c.413G>T r.(?) p.(Gly138Val)
-?/. - c.415T>C r.(?) p.(Cys139Arg)
-?/. - c.477G>T r.(?) p.(Pro159=)
?/. - c.521C>A r.(?) p.(Pro174Gln)
-?/. - c.521C>A r.(?) p.(Pro174Gln)
-?/. - c.1036A>T r.(?) p.(Thr346Ser)
-?/. - c.1175T>C r.(?) p.(Val392Ala)
-?/. - c.1210G>A r.(?) p.(Glu404Lys)
-/. - c.1230C>T r.(?) p.(Ser410=)
-/. - c.1275C>G r.(?) p.(Leu425=)
?/. - c.1606G>A r.(?) p.(Ala536Thr)
-/. 1 c.1666C>G r.(?) p.(L556V)
-/. 1 c.1666C>G r.(?) p.(L556V)
?/. 1 c.1666C>G r.(?) p.(L556V)
-/. - c.1666C>G r.(?) p.(Leu556Val)
?/. - c.1681_1683del r.(?) p.(Asn561del)
-?/. - c.1759A>G r.(?) p.(Ile587Val)
-/. - c.1776G>A r.(?) p.(=)
?/. - c.1942G>A r.(?) p.(Glu648Lys)
-/. 1 c.1991C>G r.(?) p.(S664W)
?/. 1 c.1991C>G r.(?) p.(S664W)
-/. - c.1991C>G r.(?) p.(Ser664Trp)
-/. - c.2274C>T r.(?) p.(=)
+/. 1 c.2318C>T r.(?) p.(Ala773Val)
?/. - c.2398G>A r.(?) p.(Glu800Lys)
?/. - c.2533T>G r.(?) p.(Tyr845Asp)
?/. - c.2675T>G r.(?) p.(Phe892Cys)
-/. - c.2961G>A r.(?) p.(Val987=)
+?/. 1 c.3068C>G r.(?) p.(Ala1023Gly)
-/. - c.3366C>G r.(?) p.(=)
?/. 1 c.3372C>G r.(?) p.(Ile1124Met)
-/. 1 c.3376T>C r.(?) p.(C1126R)
?/. 1 c.3376T>C r.(?) p.(C1126R)
-/. - c.3376T>C r.(?) p.(Cys1126Arg)
-?/. - c.3559G>A r.(?) p.(Val1187Ile)
-/. - c.3564G>A r.(?) p.(=)
-/. - c.3699C>G r.(?) p.(Ala1233=)
-?/. 2 c.3724G>A r.(?) p.(V1242I)
?/. 2 c.3724G>A r.(?) p.(V1242I)
-/. - c.3724G>A r.(?) p.(Val1242Ile)
?/. - c.3815G>A r.(?) p.(Gly1272Asp)
?/. - c.3953G>A r.(?) p.(Cys1318Tyr)
-?/. - c.4036G>A r.(?) p.(Gly1346Ser)
-?/. - c.4060G>A r.(?) p.(Gly1354Ser)
+?/. - c.4072_4097dup r.(?) p.(Cys1367Thrfs*62)
+?/. 2 c.4085C>T r.(?) p.(Thr1362Met)
-/. - c.4183+10C>T r.(=) p.(=)
?/. 3 c.4228G>A r.(?) p.(Gly1410Arg)
-/. - c.4518T>C r.(?) p.(Ser1506=)
-/. - c.4524C>T r.(?) p.(Gly1508=)
?/. - c.4568G>C r.(?) p.(Ser1523Thr)
+?/. - c.4613C>T r.(?) p.(Pro1538Leu)
?/. - c.4745A>G r.(?) p.(Gln1582Arg)
?/. - c.4912G>A r.(?) p.(Ala1638Thr)
?/. 7 c.4927C>T r.(?) p.(Arg1643Trp)
-/. - c.4933+19del r.(=) p.(=)
-/. 8 c.4939G>A r.(?) p.(A1647T)
?/. 8 c.4939G>A r.(?) p.(A1647T)
-/. - c.4939G>A r.(?) p.(Ala1647Thr)
+?/. 8 c.5052_5053dup r.(?) p.(Glu1685Valfs*22)
-/. - c.5112C>T r.(?) p.(=)
-?/. - c.5227-5T>C r.spl? p.?
-?/. - c.5442C>T r.(?) p.(Pro1814=)
?/. 11 c.5461G>T r.(?) p.(Val1821Leu)
-/. - c.5472A>G r.(?) p.(Gly1824=)
?/. 11 c.5473G>A r.(?) p.(Gly1825Ser)
-?/. - c.5651A>G r.(?) p.(Asn1884Ser)
-/. - c.5680T>C r.(?) p.(Tyr1894His)
+?/. 10 c.5723_5724del r.(?) p.(Val1908Glyfs*38)
?/. - c.5929G>A r.(?) p.(Asp1977Asn)
-/. - c.5964+10C>A r.(=) p.(=)
-/. 15 c.5981T>C r.(?) p.(L1994P)
?/. 15 c.5981T>C r.(?) p.(L1994P)
-/. - c.5981T>C r.(?) p.(Leu1994Pro)
-/. 15 c.5984T>C r.(?) p.(L1995P)
?/. 15 c.5984T>C r.(?) p.(L1995P)
-/. - c.5984T>C r.(?) p.(Leu1995Pro)
?/. - c.6058G>A r.(?) p.(Gly2020Arg)
-?/. - c.6123C>T r.(?) p.(=)
?/. 16 c.6184G>A r.(?) p.(Gly2062Ser)
-/. 17 c.6319A>G r.(?) p.(I2107V)
?/. 17 c.6319A>G r.(?) p.(I2107V)
-/. - c.6319A>G r.(?) p.(Ile2107Val)
?/. - c.6361C>T r.(?) p.(Arg2121Cys)
-/. - c.6441G>A r.(?) p.(Thr2147=)
-?/. - c.6576C>T r.(?) p.(Ser2192=)
-/. 19 c.6656G>A r.(?) p.(R2219H)
-?/. 19 c.6656G>A r.(?) p.(R2219H)
?/. 19 c.6656G>A r.(?) p.(R2219H)
-/. - c.6656G>A r.(?) p.(Arg2219His)
-?/. - c.6664G>C r.(?) p.(Gly2222Arg)
-/. - c.6750C>T r.(?) p.(=)
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