Canonical Allele Identifier: CA1268208113

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575098A= , CM000664.2:g.88575098A=	GRCh38
NC_000002.11:g.88874616A= , CM000664.1:g.88874616A=	GRCh37
NC_000002.10:g.88655731A=	NCBI36
NG_016424.1:g.57479T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2213T=
ENST00000682276.1:n.1830T=
ENST00000682892.1:c.1932T=	ENSP00000507214.1:p.Tyr644=
ENST00000682952.1:n.2024T=
ENST00000684455.1:c.1598T=
ENST00000684642.1:c.1782T=	ENSP00000507355.1:p.Tyr594=
ENST00000684740.1:n.2563T=
ENST00000303236.9:c.2385T= MANE Select	ENSP00000307235.3:p.Tyr795=
ENST00000652099.1:c.2579T=
ENST00000652736.1:n.2261T=
ENST00000303236.7:c.2385T=	ENSP00000307235.3:p.Tyr795=
ENST00000415570.1:c.2022T=	ENSP00000412076.1:p.Tyr674=
ENST00000419748.5:c.1932T=	ENSP00000408325.1:p.Tyr644=
ENST00000470706.1:n.49-21T=
NM_001313915.1:c.1932T=	NP_001300844.1:p.Tyr644=
NM_004836.5:c.2385T=	NP_004827.4:p.Tyr795=
NM_004836.6:c.2385T=	NP_004827.4:p.Tyr795=
NR_110236.1:n.1235A=
XM_005264649.3:c.1701T=	XP_005264706.1:p.Tyr567=
XM_017005376.2:c.1701T=	XP_016860865.1:p.Tyr567=
NM_004836.7:c.2385T= MANE Select	NP_004827.4:p.Tyr795=
NM_001313915.2:c.1932T=	NP_001300844.1:p.Tyr644=