Canonical Allele Identifier: CA350286290

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202072838T>G (hg19) ; chr2:g.201208115T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208115T>G , CM000664.2:g.201208115T>G	GRCh38
NC_000002.11:g.202072838T>G , CM000664.1:g.202072838T>G	GRCh37
NC_000002.10:g.201781083T>G	NCBI36
NG_007265.1:g.29984T>G , LRG_33:g.29984T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-955T>G	ENSP00000314599.7:n.722-955T>G
ENST00000346817.10:c.725T>G	ENSP00000237865.7:p.Leu242Arg
ENST00000438843.6:c.*311T>G	ENSP00000401914.1:n.*311T>G
ENST00000492363.6:c.762T>G	ENSP00000512459.1:p.Pro254=
ENST00000696199.1:c.721+4349T>G	ENSP00000512481.1:n.721+4349T>G
ENST00000286186.11:c.854T>G MANE Select	ENSP00000286186.6:p.Leu285Arg
ENST00000272879.9:c.854T>G	ENSP00000272879.5:p.Leu285Arg
ENST00000286186.10:c.854T>G	ENSP00000286186.6:p.Leu285Arg
ENST00000313728.11:c.722-955T>G	ENSP00000314599.7:n.722-955T>G
ENST00000346817.9:c.725T>G	ENSP00000237865.7:p.Leu242Arg
ENST00000360132.7:c.762T>G	ENSP00000353250.3:p.Pro254=
ENST00000438843.5:c.*311T>G	ENSP00000401914.1:n.*311T>G
ENST00000448480.1:c.725T>G	ENSP00000396835.1:p.Leu242Arg
ENST00000492363.5:n.762T>G
NM_001206524.1:c.722-955T>G	NP_001193453.1:n.722-955T>G
NM_001206542.1:c.725T>G	NP_001193471.1:p.Leu242Arg
NM_001230.4:c.725T>G	NP_001221.2:p.Leu242Arg
NM_032974.4:c.854T>G	NP_116756.2:p.Leu285Arg
NM_032976.3:c.762T>G	NP_116758.1:p.Pro254=
NM_032977.3:c.854T>G , LRG_33t1:c.854T>G	NP_116759.2:p.Leu285Arg
XM_005246907.2:c.851T>G	XP_005246964.1:p.Leu284Arg
XM_006712796.2:c.104T>G	XP_006712859.1:p.Leu35Arg
XM_011511990.1:c.759T>G	XP_011510292.1:p.Pro253=
XR_923043.1:n.1058T>G
XR_923044.1:n.966T>G
XM_006712796.3:c.104T>G	XP_006712859.1:p.Leu35Arg
XM_011511990.2:c.759T>G	XP_011510292.1:p.Pro253=
XR_923043.2:n.1058T>G
XR_923044.2:n.966T>G
NM_001206524.2:c.722-955T>G	NP_001193453.1:n.722-955T>G
NM_001206542.2:c.725T>G	NP_001193471.1:p.Leu242Arg
NM_001230.5:c.725T>G	NP_001221.2:p.Leu242Arg
NM_032974.5:c.854T>G	NP_116756.2:p.Leu285Arg
NM_032977.4:c.854T>G MANE Select	NP_116759.2:p.Leu285Arg
NM_032976.4:c.762T>G	NP_116758.1:p.Pro254=