Transcript #00005342 (NM_004859.3, CLTC gene)

Transcript name clathrin, heavy chain (Hc)
Gene name CLTC (clathrin, heavy chain (Hc))
Chromosome 17
Transcript - NCBI ID NM_004859.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_004850.1
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

73 entries on 1 page. Showing entries 1 - 73.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.42+4C>A r.spl? p.?
?/. - c.175A>G r.(?) p.(Ser59Gly)
?/. - c.245T>C r.(?) p.(Leu82Pro)
?/. - c.326C>A r.(?) p.(Thr109Asn)
?/. - c.368C>T r.(?) p.(Thr123Met)
?/. - c.369G>A r.(?) p.(Thr123=)
+?/. 3 c.369G>A r.[251_370del,=] p.[Ala84_Thr123del,=]
-?/. - c.796-4G>A r.spl? p.?
+/. - c.798del r.(?) p.(Ser267Valfs*9)
-?/. - c.877A>G r.(?) p.(Ile293Val)
+/. - c.977_980del r.(?) p.(Ser326Cysfs*8)
?/. - c.1162C>T r.(?) p.(Pro388Ser)
?/. - c.1177C>T r.(?) p.(Arg393Cys)
+/. - c.1226del r.(?) p.(Gly409ValfsTer25)
+/. - c.1274_1287del r.(?) p.(Gly425Valfs*8)
-?/. - c.1368+4C>T r.spl? p.?
-?/. - c.1368+5G>A r.spl? p.?
?/. - c.1618G>T r.(?) p.(Glu540Ter)
?/. - c.1647T>G r.(?) p.(Ile549Met)
+?/. - c.1660_1668del r.(?) p.(Met554_Tyr556del)
?/. - c.1745C>T r.(?) p.(Thr582Met)
+?/. - c.2272C>T r.(?) p.(Arg758Ter)
+?/. - c.2669C>T r.(?) p.(Pro890Leu)
+?/. - c.2669C>T r.(?) p.(Pro890Leu)
+?/. - c.2669C>T r.(?) p.(Pro890Leu)
?/. - c.2669C>T r.(?) p.(Pro890Leu)
+/. - c.2669C>T r.(?) p.(Pro890Leu)
+?/. - c.2737_2738dup r.(?) p.(Asp913Glufs*59)
?/. - c.2822A>C r.(?) p.(Lys941Thr)
?/. - c.2930C>T r.(?) p.(Thr977Ile)
+?/. - c.2966_2969del r.(?) p.(Ser989*)
+/. - c.3073C>T r.(?) p.(Gln1025*)
+?/. - c.3140T>C r.(?) p.(Leu1047Pro)
?/. - c.3200A>C r.(?) p.(Glu1067Ala)
?/. - c.3249+1_3249+2dup r.spl? p.?
+?/. - c.3322T>C r.(?) p.(Trp1108Arg)
?/. - c.3331C>T r.(?) p.(Leu1111Phe)
+/. - c.3595C>T r.(?) p.(Gln1199*)
+?/. - c.3621_3623del r.(?) p.(Asp1207del)
?/. - c.3698A>T r.(?) p.(His1233Leu)
+?/. - c.3766-2A>G r.spl? p.?
+?/. - c.3779G>A r.(?) p.(Cys1260Tyr)
+/. - c.3825_3826delinsAAT r.(?) p.(His1275Glnfs*8)
?/. - c.3841G>C r.(?) p.(Asp1281His)
-?/. - c.3902C>T r.(?) p.(Thr1301Ile)
?/. - c.3937C>G r.(?) p.(His1313Asp)
+?/. - c.3937C>G r.(?) p.(His1313Asp)
+/. - c.3975dup r.(?) p.(Lys1326*)
?/. - c.4255T>G r.(?) p.(Leu1419Val)
+/. - c.4400_4401del r.(?) p.(Leu1467*)
?/. - c.4435-343G>A r.(=) p.(=)
-?/. - c.4493G>A r.(?) p.(Arg1498His)
-?/. - c.4493G>A r.(?) p.(Arg1498His)
+?/. 29 c.4515del r.(?) p.(Ile1505Metfs*21)
?/. - c.4559G>T r.(?) p.(Arg1520Leu)
+/. - c.4575dup r.(?) p.(Glu1526Argfs*18)
+?/. - c.4605+2T>C r.spl p.?
?/. - c.4615C>T r.(?) p.(Gln1539Ter)
+/. - c.4663C>T r.(?) p.(Gln1555*)
+/. - c.4667G>A r.(?) p.(Trp1556*)
-?/. - c.4688G>A r.(?) p.(Arg1563Lys)
?/. - c.4702G>C r.(?) p.(Ala1568Pro)
+/. - c.4716_4717del r.(?) p.(Cys1573LeufsTer39)
-?/. - c.4870_4872del r.(?) p.(Glu1624del)
-?/. - c.4904-8T>C r.(=) p.(=)
?/. - c.*3610T>G r.(=) p.(=)
+?/. - c.*3616del r.(?) p.(=)
?/. - c.*3787G>C r.(=) p.(=)
?/. - c.*3835G>A r.(=) p.(=)
+/. - c.*3857_*3858del r.(=) p.(=)
?/. - c.*3873T>G r.(=) p.(=)
-?/. - c.*4066C>T r.(=) p.(=)
-?/. - c.*4076G>A r.(=) p.(=)
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