Canonical Allele Identifier: CA1320967350
Gene: CASP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201209388C= , CM000664.2:g.201209388C= GRCh38
NC_000002.11:g.202074111C= , CM000664.1:g.202074111C= GRCh37
NC_000002.10:g.201782356C= NCBI36
NG_007265.1:g.31257C= , LRG_33:g.31257C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.1040C= ENSP00000314599.7:p.Ala347=
ENST00000346817.10:c.1112C= ENSP00000237865.7:p.Ala371=
ENST00000438843.6:c.*698C= ENSP00000401914.1:n.*698C=
ENST00000492363.6:c.*327C= ENSP00000512459.1:n.*327C=
ENST00000696199.1:c.721+5622C= ENSP00000512481.1:n.721+5622C=
ENST00000286186.11:c.1241C= MANE Select ENSP00000286186.6:p.Ala414=
ENST00000272879.9:c.1241C= ENSP00000272879.5:p.Ala414=
ENST00000286186.10:c.1241C= ENSP00000286186.6:p.Ala414=
ENST00000313728.11:c.1040C= ENSP00000314599.7:p.Ala347=
ENST00000346817.9:c.1112C= ENSP00000237865.7:p.Ala371=
ENST00000360132.7:c.*327C= ENSP00000353250.3:n.*327C=
ENST00000448480.1:c.1112C= ENSP00000396835.1:p.Ala371=
ENST00000492363.5:n.1149C=
NM_001206524.1:c.1040C= NP_001193453.1:p.Ala347=
NM_001206542.1:c.1112C= NP_001193471.1:p.Ala371=
NM_001230.4:c.1112C= NP_001221.2:p.Ala371=
NM_032974.4:c.1241C= NP_116756.2:p.Ala414=
NM_032976.3:c.*327C= NP_116758.1:n.*327C=
NM_032977.3:c.1241C= , LRG_33t1:c.1241C= NP_116759.2:p.Ala414=
XM_005246907.2:c.1238C= XP_005246964.1:p.Ala413=
XM_006712796.2:c.491C= XP_006712859.1:p.Ala164=
XM_006712796.3:c.491C= XP_006712859.1:p.Ala164=
NM_001206524.2:c.1040C= NP_001193453.1:p.Ala347=
NM_001206542.2:c.1112C= NP_001193471.1:p.Ala371=
NM_001230.5:c.1112C= NP_001221.2:p.Ala371=
NM_032974.5:c.1241C= NP_116756.2:p.Ala414=
NM_032977.4:c.1241C= MANE Select NP_116759.2:p.Ala414=
NM_032976.4:c.*327C= NP_116758.1:n.*327C=