Canonical Allele Identifier: CA2573134332

Gene: CASP10

Linked Data

• ClinVar Variation Id: 1542333
• ClinVar RCV Id: RCV002157639
• dbSNP Id: rs2126045790
• gnomAD v4: 2-201208066-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201208066T>C , CM000664.2:g.201208066T>C	GRCh38
NC_000002.11:g.202072789T>C , CM000664.1:g.202072789T>C	GRCh37
NC_000002.10:g.201781034T>C	NCBI36
NG_007265.1:g.29935T>C , LRG_33:g.29935T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.722-1004T>C	ENSP00000314599.7:n.722-1004T>C
ENST00000346817.10:c.685-9T>C	ENSP00000237865.7:n.685-9T>C
ENST00000438843.6:c.*271-9T>C	ENSP00000401914.1:n.*271-9T>C
ENST00000492363.6:c.722-9T>C	ENSP00000512459.1:n.722-9T>C
ENST00000696199.1:c.721+4300T>C	ENSP00000512481.1:n.721+4300T>C
ENST00000286186.11:c.814-9T>C MANE Select	ENSP00000286186.6:n.814-9T>C
ENST00000272879.9:c.814-9T>C	ENSP00000272879.5:n.814-9T>C
ENST00000286186.10:c.814-9T>C	ENSP00000286186.6:n.814-9T>C
ENST00000313728.11:c.722-1004T>C	ENSP00000314599.7:n.722-1004T>C
ENST00000346817.9:c.685-9T>C	ENSP00000237865.7:n.685-9T>C
ENST00000360132.7:c.722-9T>C	ENSP00000353250.3:n.722-9T>C
ENST00000438843.5:c.*271-9T>C	ENSP00000401914.1:n.*271-9T>C
ENST00000448480.1:c.685-9T>C	ENSP00000396835.1:n.685-9T>C
ENST00000492363.5:n.722-9T>C
NM_001206524.1:c.722-1004T>C	NP_001193453.1:n.722-1004T>C
NM_001206542.1:c.685-9T>C	NP_001193471.1:n.685-9T>C
NM_001230.4:c.685-9T>C	NP_001221.2:n.685-9T>C
NM_032974.4:c.814-9T>C	NP_116756.2:n.814-9T>C
NM_032976.3:c.722-9T>C	NP_116758.1:n.722-9T>C
NM_032977.3:c.814-9T>C , LRG_33t1:c.814-9T>C	NP_116759.2:n.814-9T>C
XM_005246907.2:c.811-9T>C	XP_005246964.1:n.811-9T>C
XM_006712796.2:c.64-9T>C	XP_006712859.1:n.64-9T>C
XM_011511990.1:c.719-9T>C	XP_011510292.1:n.719-9T>C
XR_923043.1:n.1018-9T>C
XR_923044.1:n.926-9T>C
XM_006712796.3:c.64-9T>C	XP_006712859.1:n.64-9T>C
XM_011511990.2:c.719-9T>C	XP_011510292.1:n.719-9T>C
XR_923043.2:n.1018-9T>C
XR_923044.2:n.926-9T>C
NM_001206524.2:c.722-1004T>C	NP_001193453.1:n.722-1004T>C
NM_001206542.2:c.685-9T>C	NP_001193471.1:n.685-9T>C
NM_001230.5:c.685-9T>C	NP_001221.2:n.685-9T>C
NM_032974.5:c.814-9T>C	NP_116756.2:n.814-9T>C
NM_032977.4:c.814-9T>C MANE Select	NP_116759.2:n.814-9T>C
NM_032976.4:c.722-9T>C	NP_116758.1:n.722-9T>C