Canonical Allele Identifier: CA1268208285

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575572A= , CM000664.2:g.88575572A=	GRCh38
NC_000002.11:g.88875090A= , CM000664.1:g.88875090A=	GRCh37
NC_000002.10:g.88656205A=	NCBI36
NG_016424.1:g.57005T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1865-126T=
ENST00000682276.1:n.1482-126T=
ENST00000682892.1:c.1584-126T=	ENSP00000507214.1:n.1584-126T=
ENST00000682952.1:n.1676-126T=
ENST00000684455.1:c.1250-126T=
ENST00000684642.1:c.1434-126T=	ENSP00000507355.1:n.1434-126T=
ENST00000684740.1:n.2215-126T=
ENST00000303236.9:c.2037-126T= MANE Select	ENSP00000307235.3:n.2037-126T=
ENST00000652099.1:c.2231-126T=
ENST00000652736.1:n.1913-126T=
ENST00000303236.7:c.2037-126T=	ENSP00000307235.3:n.2037-126T=
ENST00000415570.1:c.1674-126T=	ENSP00000412076.1:n.1674-126T=
ENST00000419748.5:c.1584-126T=	ENSP00000408325.1:n.1584-126T=
ENST00000478003.1:n.603-126T=
NM_001313915.1:c.1584-126T=	NP_001300844.1:n.1584-126T=
NM_004836.5:c.2037-126T=	NP_004827.4:n.2037-126T=
NM_004836.6:c.2037-126T=	NP_004827.4:n.2037-126T=
NR_110236.1:n.1709A=
XM_005264649.3:c.1353-126T=	XP_005264706.1:n.1353-126T=
XR_939749.1:n.2316-126T=
XM_017005376.2:c.1353-126T=	XP_016860865.1:n.1353-126T=
NM_004836.7:c.2037-126T= MANE Select	NP_004827.4:n.2037-126T=
NM_001313915.2:c.1584-126T=	NP_001300844.1:n.1584-126T=