Canonical Allele Identifier: CA430614388

Gene: CASP10

Linked Data

• MyVariant Identifiers: chr2:g.202073926G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.201209203G>A , CM000664.2:g.201209203G>A	GRCh38
NC_000002.11:g.202073926G>A , CM000664.1:g.202073926G>A	GRCh37
NC_000002.10:g.201782171G>A	NCBI36
NG_007265.1:g.31072G>A , LRG_33:g.31072G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000313728.12:c.855G>A	ENSP00000314599.7:p.Val285=
ENST00000346817.10:c.927G>A	ENSP00000237865.7:p.Val309=
ENST00000438843.6:c.*513G>A	ENSP00000401914.1:n.*513G>A
ENST00000492363.6:c.*142G>A	ENSP00000512459.1:n.*142G>A
ENST00000696199.1:c.721+5437G>A	ENSP00000512481.1:n.721+5437G>A
ENST00000286186.11:c.1056G>A MANE Select	ENSP00000286186.6:p.Val352=
ENST00000272879.9:c.1056G>A	ENSP00000272879.5:p.Val352=
ENST00000286186.10:c.1056G>A	ENSP00000286186.6:p.Val352=
ENST00000313728.11:c.855G>A	ENSP00000314599.7:p.Val285=
ENST00000346817.9:c.927G>A	ENSP00000237865.7:p.Val309=
ENST00000360132.7:c.*142G>A	ENSP00000353250.3:n.*142G>A
ENST00000448480.1:c.927G>A	ENSP00000396835.1:p.Val309=
ENST00000492363.5:n.964G>A
NM_001206524.1:c.855G>A	NP_001193453.1:p.Val285=
NM_001206542.1:c.927G>A	NP_001193471.1:p.Val309=
NM_001230.4:c.927G>A	NP_001221.2:p.Val309=
NM_032974.4:c.1056G>A	NP_116756.2:p.Val352=
NM_032976.3:c.*142G>A	NP_116758.1:n.*142G>A
NM_032977.3:c.1056G>A , LRG_33t1:c.1056G>A	NP_116759.2:p.Val352=
XM_005246907.2:c.1053G>A	XP_005246964.1:p.Val351=
XM_006712796.2:c.306G>A	XP_006712859.1:p.Val102=
XM_006712796.3:c.306G>A	XP_006712859.1:p.Val102=
NM_001206524.2:c.855G>A	NP_001193453.1:p.Val285=
NM_001206542.2:c.927G>A	NP_001193471.1:p.Val309=
NM_001230.5:c.927G>A	NP_001221.2:p.Val309=
NM_032974.5:c.1056G>A	NP_116756.2:p.Val352=
NM_032977.4:c.1056G>A MANE Select	NP_116759.2:p.Val352=
NM_032976.4:c.*142G>A	NP_116758.1:n.*142G>A