Canonical Allele Identifier: CA1320967386

Gene: CASP10

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209462G= , CM000664.2:g.201209462G=	GRCh38
NC_000002.11:g.202074185G= , CM000664.1:g.202074185G=	GRCh37
NC_000002.10:g.201782430G=	NCBI36
NG_007265.1:g.31331G= , LRG_33:g.31331G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1114G=	ENSP00000314599.7:p.Gly372=
ENST00000346817.10:c.1186G=	ENSP00000237865.7:p.Gly396=
ENST00000438843.6:c.*772G=	ENSP00000401914.1:n.*772G=
ENST00000492363.6:c.*401G=	ENSP00000512459.1:n.*401G=
ENST00000696199.1:c.721+5696G=	ENSP00000512481.1:n.721+5696G=
ENST00000286186.11:c.1315G= MANE Select	ENSP00000286186.6:p.Gly439=
ENST00000272879.9:c.1315G=	ENSP00000272879.5:p.Gly439=
ENST00000286186.10:c.1315G=	ENSP00000286186.6:p.Gly439=
ENST00000313728.11:c.1114G=	ENSP00000314599.7:p.Gly372=
ENST00000346817.9:c.1186G=	ENSP00000237865.7:p.Gly396=
ENST00000360132.7:c.*401G=	ENSP00000353250.3:n.*401G=
ENST00000448480.1:c.1186G=	ENSP00000396835.1:p.Gly396=
ENST00000492363.5:n.1223G=
NM_001206524.1:c.1114G=	NP_001193453.1:p.Gly372=
NM_001206542.1:c.1186G=	NP_001193471.1:p.Gly396=
NM_001230.4:c.1186G=	NP_001221.2:p.Gly396=
NM_032974.4:c.1315G=	NP_116756.2:p.Gly439=
NM_032976.3:c.*401G=	NP_116758.1:n.*401G=
NM_032977.3:c.1315G= , LRG_33t1:c.1315G=	NP_116759.2:p.Gly439=
XM_005246907.2:c.1312G=	XP_005246964.1:p.Gly438=
XM_006712796.2:c.565G=	XP_006712859.1:p.Gly189=
XM_006712796.3:c.565G=	XP_006712859.1:p.Gly189=
NM_001206524.2:c.1114G=	NP_001193453.1:p.Gly372=
NM_001206542.2:c.1186G=	NP_001193471.1:p.Gly396=
NM_001230.5:c.1186G=	NP_001221.2:p.Gly396=
NM_032974.5:c.1315G=	NP_116756.2:p.Gly439=
NM_032977.4:c.1315G= MANE Select	NP_116759.2:p.Gly439=
NM_032976.4:c.*401G=	NP_116758.1:n.*401G=