Canonical Allele Identifier: CA1320967359
Gene: CASP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201209416C= , CM000664.2:g.201209416C= GRCh38
NC_000002.11:g.202074139C= , CM000664.1:g.202074139C= GRCh37
NC_000002.10:g.201782384C= NCBI36
NG_007265.1:g.31285C= , LRG_33:g.31285C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000313728.12:c.1068C= ENSP00000314599.7:p.Pro356=
ENST00000346817.10:c.1140C= ENSP00000237865.7:p.Pro380=
ENST00000438843.6:c.*726C= ENSP00000401914.1:n.*726C=
ENST00000492363.6:c.*355C= ENSP00000512459.1:n.*355C=
ENST00000696199.1:c.721+5650C= ENSP00000512481.1:n.721+5650C=
ENST00000286186.11:c.1269C= MANE Select ENSP00000286186.6:p.Pro423=
ENST00000272879.9:c.1269C= ENSP00000272879.5:p.Pro423=
ENST00000286186.10:c.1269C= ENSP00000286186.6:p.Pro423=
ENST00000313728.11:c.1068C= ENSP00000314599.7:p.Pro356=
ENST00000346817.9:c.1140C= ENSP00000237865.7:p.Pro380=
ENST00000360132.7:c.*355C= ENSP00000353250.3:n.*355C=
ENST00000448480.1:c.1140C= ENSP00000396835.1:p.Pro380=
ENST00000492363.5:n.1177C=
NM_001206524.1:c.1068C= NP_001193453.1:p.Pro356=
NM_001206542.1:c.1140C= NP_001193471.1:p.Pro380=
NM_001230.4:c.1140C= NP_001221.2:p.Pro380=
NM_032974.4:c.1269C= NP_116756.2:p.Pro423=
NM_032976.3:c.*355C= NP_116758.1:n.*355C=
NM_032977.3:c.1269C= , LRG_33t1:c.1269C= NP_116759.2:p.Pro423=
XM_005246907.2:c.1266C= XP_005246964.1:p.Pro422=
XM_006712796.2:c.519C= XP_006712859.1:p.Pro173=
XM_006712796.3:c.519C= XP_006712859.1:p.Pro173=
NM_001206524.2:c.1068C= NP_001193453.1:p.Pro356=
NM_001206542.2:c.1140C= NP_001193471.1:p.Pro380=
NM_001230.5:c.1140C= NP_001221.2:p.Pro380=
NM_032974.5:c.1269C= NP_116756.2:p.Pro423=
NM_032977.4:c.1269C= MANE Select NP_116759.2:p.Pro423=
NM_032976.4:c.*355C= NP_116758.1:n.*355C=