Canonical Allele Identifier: CA430829695

Gene: CASP10

Linked Data

• gnomAD v4: 2-201209473-T-G
• MyVariant Identifiers: chr2:g.202074196T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209473T>G , CM000664.2:g.201209473T>G	GRCh38
NC_000002.11:g.202074196T>G , CM000664.1:g.202074196T>G	GRCh37
NC_000002.10:g.201782441T>G	NCBI36
NG_007265.1:g.31342T>G , LRG_33:g.31342T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1125T>G	ENSP00000314599.7:p.Thr375=
ENST00000346817.10:c.1197T>G	ENSP00000237865.7:p.Thr399=
ENST00000438843.6:c.*783T>G	ENSP00000401914.1:n.*783T>G
ENST00000492363.6:c.*412T>G	ENSP00000512459.1:n.*412T>G
ENST00000696199.1:c.721+5707T>G	ENSP00000512481.1:n.721+5707T>G
ENST00000286186.11:c.1326T>G MANE Select	ENSP00000286186.6:p.Thr442=
ENST00000272879.9:c.1326T>G	ENSP00000272879.5:p.Thr442=
ENST00000286186.10:c.1326T>G	ENSP00000286186.6:p.Thr442=
ENST00000313728.11:c.1125T>G	ENSP00000314599.7:p.Thr375=
ENST00000346817.9:c.1197T>G	ENSP00000237865.7:p.Thr399=
ENST00000360132.7:c.*412T>G	ENSP00000353250.3:n.*412T>G
ENST00000448480.1:c.1197T>G	ENSP00000396835.1:p.Thr399=
ENST00000492363.5:n.1234T>G
NM_001206524.1:c.1125T>G	NP_001193453.1:p.Thr375=
NM_001206542.1:c.1197T>G	NP_001193471.1:p.Thr399=
NM_001230.4:c.1197T>G	NP_001221.2:p.Thr399=
NM_032974.4:c.1326T>G	NP_116756.2:p.Thr442=
NM_032976.3:c.*412T>G	NP_116758.1:n.*412T>G
NM_032977.3:c.1326T>G , LRG_33t1:c.1326T>G	NP_116759.2:p.Thr442=
XM_005246907.2:c.1323T>G	XP_005246964.1:p.Thr441=
XM_006712796.2:c.576T>G	XP_006712859.1:p.Thr192=
XM_006712796.3:c.576T>G	XP_006712859.1:p.Thr192=
NM_001206524.2:c.1125T>G	NP_001193453.1:p.Thr375=
NM_001206542.2:c.1197T>G	NP_001193471.1:p.Thr399=
NM_001230.5:c.1197T>G	NP_001221.2:p.Thr399=
NM_032974.5:c.1326T>G	NP_116756.2:p.Thr442=
NM_032977.4:c.1326T>G MANE Select	NP_116759.2:p.Thr442=
NM_032976.4:c.*412T>G	NP_116758.1:n.*412T>G