Canonical Allele Identifier: CA350286404

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202072849G>C (hg19) ; chr2:g.201208126G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208126G>C , CM000664.2:g.201208126G>C	GRCh38
NC_000002.11:g.202072849G>C , CM000664.1:g.202072849G>C	GRCh37
NC_000002.10:g.201781094G>C	NCBI36
NG_007265.1:g.29995G>C , LRG_33:g.29995G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-944G>C	ENSP00000314599.7:n.722-944G>C
ENST00000346817.10:c.736G>C	ENSP00000237865.7:p.Val246Leu
ENST00000438843.6:c.*322G>C	ENSP00000401914.1:n.*322G>C
ENST00000492363.6:c.773G>C	ENSP00000512459.1:p.Cys258Ser
ENST00000696199.1:c.721+4360G>C	ENSP00000512481.1:n.721+4360G>C
ENST00000286186.11:c.865G>C MANE Select	ENSP00000286186.6:p.Val289Leu
ENST00000272879.9:c.865G>C	ENSP00000272879.5:p.Val289Leu
ENST00000286186.10:c.865G>C	ENSP00000286186.6:p.Val289Leu
ENST00000313728.11:c.722-944G>C	ENSP00000314599.7:n.722-944G>C
ENST00000346817.9:c.736G>C	ENSP00000237865.7:p.Val246Leu
ENST00000360132.7:c.773G>C	ENSP00000353250.3:p.Cys258Ser
ENST00000438843.5:c.*322G>C	ENSP00000401914.1:n.*322G>C
ENST00000448480.1:c.736G>C	ENSP00000396835.1:p.Val246Leu
ENST00000492363.5:n.773G>C
NM_001206524.1:c.722-944G>C	NP_001193453.1:n.722-944G>C
NM_001206542.1:c.736G>C	NP_001193471.1:p.Val246Leu
NM_001230.4:c.736G>C	NP_001221.2:p.Val246Leu
NM_032974.4:c.865G>C	NP_116756.2:p.Val289Leu
NM_032976.3:c.773G>C	NP_116758.1:p.Cys258Ser
NM_032977.3:c.865G>C , LRG_33t1:c.865G>C	NP_116759.2:p.Val289Leu
XM_005246907.2:c.862G>C	XP_005246964.1:p.Val288Leu
XM_006712796.2:c.115G>C	XP_006712859.1:p.Val39Leu
XM_011511990.1:c.770G>C	XP_011510292.1:p.Cys257Ser
XR_923043.1:n.1069G>C
XR_923044.1:n.977G>C
XM_006712796.3:c.115G>C	XP_006712859.1:p.Val39Leu
XM_011511990.2:c.770G>C	XP_011510292.1:p.Cys257Ser
XR_923043.2:n.1069G>C
XR_923044.2:n.977G>C
NM_001206524.2:c.722-944G>C	NP_001193453.1:n.722-944G>C
NM_001206542.2:c.736G>C	NP_001193471.1:p.Val246Leu
NM_001230.5:c.736G>C	NP_001221.2:p.Val246Leu
NM_032974.5:c.865G>C	NP_116756.2:p.Val289Leu
NM_032977.4:c.865G>C MANE Select	NP_116759.2:p.Val289Leu
NM_032976.4:c.773G>C	NP_116758.1:p.Cys258Ser