Transcript #00005701 (NM_006371.4, CRTAP gene)

Transcript name cartilage associated protein
Gene name CRTAP (cartilage associated protein)
Chromosome 3
Transcript - NCBI ID NM_006371.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_006362.1
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

75 entries on 1 page. Showing entries 1 - 75.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/+ _1_1i c.-1677_471+1592del r.0? p.0?
+/+ 1 c.3G>A r.(?) p.(Met1?)
+/. 1 c.21_22dup r.(?) p.(Ala8GlyfsTer6)
+/. - c.21_22dup r.(?) p.(Ala8GlyfsTer6)
+/+ 1 c.21_22dup r.(?) p.(Ala8Glyfs*6)
+/+ 1 c.22dup r.(?) p.(Ala8Glyfs*153)
+/+ 1 c.24_31del r.(?) p.(Ala10Serfs*148)
?/? 1 c.38C>A r.(?) p.(Ala13Glu)
+/. - c.62_77del r.(?) p.(Leu21Profs*16)
?/. - c.101_109dup r.(?) p.(Arg34_Phe36dup)
+/. 1 c.118G>T r.(?) p.(Glu40*)
+/+ 1 c.118_133delinsTACCC r.(?) p.(Glu40Tyrfs*117)
+/+ 1 c.133G>T r.(?) p.(Glu45*)
+?/. - c.160_167del r.(?) p.(Lys54Argfs*104)
+/+ 1 c.198C>A r.(?) p.(Tyr66*)
+?/. - c.200T>C r.(?) p.(Leu67Pro)
+/+ 1 c.200T>C r.(?) p.(Leu67Pro)
+/+ 1 c.202G>T r.(?) p.(Glu68*)
-/. - c.213G>A r.(?) p.(Leu71=)
-/. - c.213G>A r.(?) p.(Leu71=)
+/+ 1 c.278_293dup r.(?) p.(Gly99Alafs*67)
+/+ 1 c.278_293dup r.(?) p.(Gly99Alafs*67)
+/+ 1 c.404del r.(?) p.Ser135Thrfs*39
+/+ 1 c.452T>C r.(?) p.(Leu151Pro)
?/? 1 c.469A>G r.(?) p.(Lys157Glu)
+/. - c.470A>G r.(?) p.(Lys157Arg)
+/+ 1i c.471+1G>C r.spl p.?
+/+ 1i c.471+2C>A r.spl p.?
+/+ 1i c.471+2C>A r.spl p.?
+/+ 1i c.471+2C>A r.spl p.?
+/+ 1i c.471+2C>A r.spl p.?
+/. - c.471+2C>A r.spl? p.?
+/+ 1i c.471+4del r.spl p.?
-?/. - c.471+7C>T r.(=) p.(=)
+/+ 1i c.472-1021C>G r.spl p.?
-/. - c.534C>T r.(?) p.(Asp178=)
-/. - c.534C>T r.(?) p.(Asp178=)
-/- 2 c.534C>T r.(?) p.(Asp174=)
+/. - c.535G>T r.(?) p.(Glu179Ter)
+?/- 2 c.558A>G r.(?) p.(Ala186=)
-/. - c.558A>G r.(?) p.(Ala186=)
+/. - c.561T>G r.(?) p.(Tyr187*)
+/+ 2 c.561T>G r.(?) p.(Tyr187*)
-?/. - c.582C>T r.(?) p.(Ala194=)
-?/. - c.622-16T>C r.(=) p.(=)
+/+ 3 c.634C>T r.(?) p.(Arg212*)
-?/. - c.641T>C r.(?) p.(Val214Ala)
-/. - c.641T>C r.(?) p.(Val214Ala)
?/. - c.724G>A r.(?) p.(Glu242Lys)
+/. - c.731_732del r.(?) p.(Leu244ArgfsTer34)
-?/. - c.732C>T r.(?) p.(Leu244=)
+/. - c.794-1403A>G r.[793_794ins794-1472_794-1404,(793_794ins[793+1_793+7;794-1472_794-1404]] p.?
+/+ 4 c.804_809del r.(?) p.Glu269_Val270del
+/+ 4 c.822_826delinsT r.(?) p.(Lys274Asnfs*11)
+/. - c.826C>T r.(?) p.(Gln276*)
+/+ 4 c.826C>T r.(?) p.(Gln276*)
+/+ 4 c.826C>T r.(?) p.(Gln276*)
+/+ 4 c.879del r.(?) p.Phe293Leufs*16
-/. - c.888C>T r.(?) p.(Thr296=)
+/+ 4i c.923-2A>G r.spl p.?
+/? 5 c.976C>T r.(?) p.(Gln326*)
+/? 5 c.976C>T r.(?) p.(Gln326*)
+?/. - c.986del r.(?) p.(Lys329Argfs*36)
-?/. - c.994C>G r.(?) p.(Gln332Glu)
-/. - c.1032T>G r.(?) p.(Thr344=)
-/. - c.1032T>G r.(?) p.(Thr344=)
?/- 5 c.1032T>G r.(?) p.(=)
?/. - c.1039C>T r.(?) p.(Leu347Phe)
-/. - c.1044G>A r.(?) p.(Ser348=)
-/. - c.1044G>A r.(?) p.(Ser348=)
?/- 5 c.1044G>A r.(?) p.(=)
+/+ 5 c.1046A>G r.(?) p.(Asp349_Pro356del)
+/+ 6 c.1112dup r.(?) p.(Tyr372Valfs*2)
-/- 6i c.1152+36C>A r.(?) p.(=)
-?/. - c.1153-8T>C r.(=) p.(=)
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