Canonical Allele Identifier: CA1320966766
Community Standard Title: NM_032977.4(CASP10):c.853C= (p.Leu285=)
Gene: CASP10 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.201208114C= , CM000664.2:g.201208114C= GRCh38
NC_000002.11:g.202072837C= , CM000664.1:g.202072837C= GRCh37
NC_000002.10:g.201781082C= NCBI36
NG_007265.1:g.29983C= , LRG_33:g.29983C=

Transcript Alleles

HGVS Amino-acid Change
NM_032977.4:c.853C= MANE Select NP_116759.2:p.Leu285=
ENST00000286186.11:c.853C= MANE Select ENSP00000286186.6:p.Leu285=
NM_001206524.1:c.722-956C= NP_001193453.1:n.722-956C=
NM_001206524.2:c.722-956C= NP_001193453.1:n.722-956C=
NM_001206542.1:c.724C= NP_001193471.1:p.Leu242=
NM_001206542.2:c.724C= NP_001193471.1:p.Leu242=
NM_001230.4:c.724C= NP_001221.2:p.Leu242=
NM_001230.5:c.724C= NP_001221.2:p.Leu242=
NM_032974.4:c.853C= NP_116756.2:p.Leu285=
NM_032974.5:c.853C= NP_116756.2:p.Leu285=
NM_032976.3:c.761C= NP_116758.1:p.Pro254=
NM_032976.4:c.761C= NP_116758.1:p.Pro254=
NM_032977.3:c.853C= , LRG_33t1:c.853C= NP_116759.2:p.Leu285=
ENST00000272879.9:c.853C= ENSP00000272879.5:p.Leu285=
ENST00000286186.10:c.853C= ENSP00000286186.6:p.Leu285=
ENST00000313728.11:c.722-956C= ENSP00000314599.7:n.722-956C=
ENST00000313728.12:c.722-956C= ENSP00000314599.7:n.722-956C=
ENST00000346817.10:c.724C= ENSP00000237865.7:p.Leu242=
ENST00000346817.9:c.724C= ENSP00000237865.7:p.Leu242=
ENST00000360132.7:c.761C= ENSP00000353250.3:p.Pro254=
ENST00000438843.5:c.*310C= ENSP00000401914.1:n.*310C=
ENST00000438843.6:c.*310C= ENSP00000401914.1:n.*310C=
ENST00000448480.1:c.724C= ENSP00000396835.1:p.Leu242=
ENST00000492363.5:n.761C=
ENST00000492363.6:c.761C= ENSP00000512459.1:p.Pro254=
ENST00000696199.1:c.721+4348C= ENSP00000512481.1:n.721+4348C=
XM_005246907.2:c.850C= XP_005246964.1:p.Leu284=
XM_006712796.2:c.103C= XP_006712859.1:p.Leu35=
XM_006712796.3:c.103C= XP_006712859.1:p.Leu35=
XM_011511990.1:c.758C= XP_011510292.1:p.Pro253=
XM_011511990.2:c.758C= XP_011510292.1:p.Pro253=
XR_923043.1:n.1057C=
XR_923043.2:n.1057C=
XR_923044.1:n.965C=
XR_923044.2:n.965C=