Canonical Allele Identifier: CA350291975

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202074059T>A (hg19) ; chr2:g.201209336T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209336T>A , CM000664.2:g.201209336T>A	GRCh38
NC_000002.11:g.202074059T>A , CM000664.1:g.202074059T>A	GRCh37
NC_000002.10:g.201782304T>A	NCBI36
NG_007265.1:g.31205T>A , LRG_33:g.31205T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000313728.12:c.988T>A	ENSP00000314599.7:p.Phe330Ile
ENST00000346817.10:c.1060T>A	ENSP00000237865.7:p.Phe354Ile
ENST00000438843.6:c.*646T>A	ENSP00000401914.1:n.*646T>A
ENST00000492363.6:c.*275T>A	ENSP00000512459.1:n.*275T>A
ENST00000696199.1:c.721+5570T>A	ENSP00000512481.1:n.721+5570T>A
ENST00000286186.11:c.1189T>A MANE Select	ENSP00000286186.6:p.Phe397Ile
ENST00000272879.9:c.1189T>A	ENSP00000272879.5:p.Phe397Ile
ENST00000286186.10:c.1189T>A	ENSP00000286186.6:p.Phe397Ile
ENST00000313728.11:c.988T>A	ENSP00000314599.7:p.Phe330Ile
ENST00000346817.9:c.1060T>A	ENSP00000237865.7:p.Phe354Ile
ENST00000360132.7:c.*275T>A	ENSP00000353250.3:n.*275T>A
ENST00000448480.1:c.1060T>A	ENSP00000396835.1:p.Phe354Ile
ENST00000492363.5:n.1097T>A
NM_001206524.1:c.988T>A	NP_001193453.1:p.Phe330Ile
NM_001206542.1:c.1060T>A	NP_001193471.1:p.Phe354Ile
NM_001230.4:c.1060T>A	NP_001221.2:p.Phe354Ile
NM_032974.4:c.1189T>A	NP_116756.2:p.Phe397Ile
NM_032976.3:c.*275T>A	NP_116758.1:n.*275T>A
NM_032977.3:c.1189T>A , LRG_33t1:c.1189T>A	NP_116759.2:p.Phe397Ile
XM_005246907.2:c.1186T>A	XP_005246964.1:p.Phe396Ile
XM_006712796.2:c.439T>A	XP_006712859.1:p.Phe147Ile
XM_006712796.3:c.439T>A	XP_006712859.1:p.Phe147Ile
NM_001206524.2:c.988T>A	NP_001193453.1:p.Phe330Ile
NM_001206542.2:c.1060T>A	NP_001193471.1:p.Phe354Ile
NM_001230.5:c.1060T>A	NP_001221.2:p.Phe354Ile
NM_032974.5:c.1189T>A	NP_116756.2:p.Phe397Ile
NM_032977.4:c.1189T>A MANE Select	NP_116759.2:p.Phe397Ile
NM_032976.4:c.*275T>A	NP_116758.1:n.*275T>A