Canonical Allele Identifier: CA350286676

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202072873C>G (hg19) ; chr2:g.201208150C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208150C>G , CM000664.2:g.201208150C>G	GRCh38
NC_000002.11:g.202072873C>G , CM000664.1:g.202072873C>G	GRCh37
NC_000002.10:g.201781118C>G	NCBI36
NG_007265.1:g.30019C>G , LRG_33:g.30019C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-920C>G	ENSP00000314599.7:n.722-920C>G
ENST00000346817.10:c.760C>G	ENSP00000237865.7:p.Leu254Val
ENST00000438843.6:c.*346C>G	ENSP00000401914.1:n.*346C>G
ENST00000492363.6:c.797C>G	ENSP00000512459.1:p.Pro266Arg
ENST00000696199.1:c.721+4384C>G	ENSP00000512481.1:n.721+4384C>G
ENST00000286186.11:c.889C>G MANE Select	ENSP00000286186.6:p.Leu297Val
ENST00000272879.9:c.889C>G	ENSP00000272879.5:p.Leu297Val
ENST00000286186.10:c.889C>G	ENSP00000286186.6:p.Leu297Val
ENST00000313728.11:c.722-920C>G	ENSP00000314599.7:n.722-920C>G
ENST00000346817.9:c.760C>G	ENSP00000237865.7:p.Leu254Val
ENST00000360132.7:c.797C>G	ENSP00000353250.3:p.Pro266Arg
ENST00000438843.5:c.*346C>G	ENSP00000401914.1:n.*346C>G
ENST00000448480.1:c.760C>G	ENSP00000396835.1:p.Leu254Val
ENST00000492363.5:n.797C>G
NM_001206524.1:c.722-920C>G	NP_001193453.1:n.722-920C>G
NM_001206542.1:c.760C>G	NP_001193471.1:p.Leu254Val
NM_001230.4:c.760C>G	NP_001221.2:p.Leu254Val
NM_032974.4:c.889C>G	NP_116756.2:p.Leu297Val
NM_032976.3:c.797C>G	NP_116758.1:p.Pro266Arg
NM_032977.3:c.889C>G , LRG_33t1:c.889C>G	NP_116759.2:p.Leu297Val
XM_005246907.2:c.886C>G	XP_005246964.1:p.Leu296Val
XM_006712796.2:c.139C>G	XP_006712859.1:p.Leu47Val
XM_011511990.1:c.794C>G	XP_011510292.1:p.Pro265Arg
XR_923043.1:n.1093C>G
XR_923044.1:n.1001C>G
XM_006712796.3:c.139C>G	XP_006712859.1:p.Leu47Val
XM_011511990.2:c.794C>G	XP_011510292.1:p.Pro265Arg
XR_923043.2:n.1093C>G
XR_923044.2:n.1001C>G
NM_001206524.2:c.722-920C>G	NP_001193453.1:n.722-920C>G
NM_001206542.2:c.760C>G	NP_001193471.1:p.Leu254Val
NM_001230.5:c.760C>G	NP_001221.2:p.Leu254Val
NM_032974.5:c.889C>G	NP_116756.2:p.Leu297Val
NM_032977.4:c.889C>G MANE Select	NP_116759.2:p.Leu297Val
NM_032976.4:c.797C>G	NP_116758.1:p.Pro266Arg