Canonical Allele Identifier: CA350293268

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202074257T>G (hg19) ; chr2:g.201209534T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209534T>G , CM000664.2:g.201209534T>G	GRCh38
NC_000002.11:g.202074257T>G , CM000664.1:g.202074257T>G	GRCh37
NC_000002.10:g.201782502T>G	NCBI36
NG_007265.1:g.31403T>G , LRG_33:g.31403T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.1186T>G	ENSP00000314599.7:p.Cys396Gly
ENST00000346817.10:c.1258T>G	ENSP00000237865.7:p.Cys420Gly
ENST00000438843.6:c.*844T>G	ENSP00000401914.1:n.*844T>G
ENST00000492363.6:c.*473T>G	ENSP00000512459.1:n.*473T>G
ENST00000696199.1:c.721+5768T>G	ENSP00000512481.1:n.721+5768T>G
ENST00000286186.11:c.1387T>G MANE Select	ENSP00000286186.6:p.Cys463Gly
ENST00000272879.9:c.1387T>G	ENSP00000272879.5:p.Cys463Gly
ENST00000286186.10:c.1387T>G	ENSP00000286186.6:p.Cys463Gly
ENST00000313728.11:c.1186T>G	ENSP00000314599.7:p.Cys396Gly
ENST00000346817.9:c.1258T>G	ENSP00000237865.7:p.Cys420Gly
ENST00000360132.7:c.*473T>G	ENSP00000353250.3:n.*473T>G
ENST00000448480.1:c.1258T>G	ENSP00000396835.1:p.Cys420Gly
ENST00000492363.5:n.1295T>G
NM_001206524.1:c.1186T>G	NP_001193453.1:p.Cys396Gly
NM_001206542.1:c.1258T>G	NP_001193471.1:p.Cys420Gly
NM_001230.4:c.1258T>G	NP_001221.2:p.Cys420Gly
NM_032974.4:c.1387T>G	NP_116756.2:p.Cys463Gly
NM_032976.3:c.*473T>G	NP_116758.1:n.*473T>G
NM_032977.3:c.1387T>G , LRG_33t1:c.1387T>G	NP_116759.2:p.Cys463Gly
XM_005246907.2:c.1384T>G	XP_005246964.1:p.Cys462Gly
XM_006712796.2:c.637T>G	XP_006712859.1:p.Cys213Gly
XM_006712796.3:c.637T>G	XP_006712859.1:p.Cys213Gly
NM_001206524.2:c.1186T>G	NP_001193453.1:p.Cys396Gly
NM_001206542.2:c.1258T>G	NP_001193471.1:p.Cys420Gly
NM_001230.5:c.1258T>G	NP_001221.2:p.Cys420Gly
NM_032974.5:c.1387T>G	NP_116756.2:p.Cys463Gly
NM_032977.4:c.1387T>G MANE Select	NP_116759.2:p.Cys463Gly
NM_032976.4:c.*473T>G	NP_116758.1:n.*473T>G