Canonical Allele Identifier: CA350286766

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202072879G>T (hg19) ; chr2:g.201208156G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208156G>T , CM000664.2:g.201208156G>T	GRCh38
NC_000002.11:g.202072879G>T , CM000664.1:g.202072879G>T	GRCh37
NC_000002.10:g.201781124G>T	NCBI36
NG_007265.1:g.30025G>T , LRG_33:g.30025G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-914G>T	ENSP00000314599.7:n.722-914G>T
ENST00000346817.10:c.766G>T	ENSP00000237865.7:p.Asp256Tyr
ENST00000438843.6:c.*352G>T	ENSP00000401914.1:n.*352G>T
ENST00000492363.6:c.803G>T	ENSP00000512459.1:p.Gly268Val
ENST00000696199.1:c.721+4390G>T	ENSP00000512481.1:n.721+4390G>T
ENST00000286186.11:c.895G>T MANE Select	ENSP00000286186.6:p.Asp299Tyr
ENST00000272879.9:c.895G>T	ENSP00000272879.5:p.Asp299Tyr
ENST00000286186.10:c.895G>T	ENSP00000286186.6:p.Asp299Tyr
ENST00000313728.11:c.722-914G>T	ENSP00000314599.7:n.722-914G>T
ENST00000346817.9:c.766G>T	ENSP00000237865.7:p.Asp256Tyr
ENST00000360132.7:c.803G>T	ENSP00000353250.3:p.Gly268Val
ENST00000438843.5:c.*352G>T	ENSP00000401914.1:n.*352G>T
ENST00000448480.1:c.766G>T	ENSP00000396835.1:p.Asp256Tyr
ENST00000492363.5:n.803G>T
NM_001206524.1:c.722-914G>T	NP_001193453.1:n.722-914G>T
NM_001206542.1:c.766G>T	NP_001193471.1:p.Asp256Tyr
NM_001230.4:c.766G>T	NP_001221.2:p.Asp256Tyr
NM_032974.4:c.895G>T	NP_116756.2:p.Asp299Tyr
NM_032976.3:c.803G>T	NP_116758.1:p.Gly268Val
NM_032977.3:c.895G>T , LRG_33t1:c.895G>T	NP_116759.2:p.Asp299Tyr
XM_005246907.2:c.892G>T	XP_005246964.1:p.Asp298Tyr
XM_006712796.2:c.145G>T	XP_006712859.1:p.Asp49Tyr
XM_011511990.1:c.800G>T	XP_011510292.1:p.Gly267Val
XR_923043.1:n.1099G>T
XR_923044.1:n.1007G>T
XM_006712796.3:c.145G>T	XP_006712859.1:p.Asp49Tyr
XM_011511990.2:c.800G>T	XP_011510292.1:p.Gly267Val
XR_923043.2:n.1099G>T
XR_923044.2:n.1007G>T
NM_001206524.2:c.722-914G>T	NP_001193453.1:n.722-914G>T
NM_001206542.2:c.766G>T	NP_001193471.1:p.Asp256Tyr
NM_001230.5:c.766G>T	NP_001221.2:p.Asp256Tyr
NM_032974.5:c.895G>T	NP_116756.2:p.Asp299Tyr
NM_032977.4:c.895G>T MANE Select	NP_116759.2:p.Asp299Tyr
NM_032976.4:c.803G>T	NP_116758.1:p.Gly268Val