Canonical Allele Identifier: CA1268211591

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88583437T= , CM000664.2:g.88583437T=	GRCh38
NC_000002.11:g.88882955T= , CM000664.1:g.88882955T=	GRCh37
NC_000002.10:g.88664070T=	NCBI36
NG_016424.1:g.49140A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682276.1:n.1201A=
ENST00000682892.1:c.1303A=	ENSP00000507214.1:p.Ile435=
ENST00000682952.1:n.1395A=
ENST00000684455.1:c.969A=
ENST00000684642.1:c.1153A=	ENSP00000507355.1:p.Ile385=
ENST00000303236.9:c.1756A= MANE Select	ENSP00000307235.3:p.Ile586=
ENST00000652099.1:c.1950A=
ENST00000652736.1:n.1632A=
ENST00000303236.7:c.1756A=	ENSP00000307235.3:p.Ile586=
ENST00000415570.1:c.1393A=	ENSP00000412076.1:p.Ile465=
ENST00000419748.5:c.1303A=	ENSP00000408325.1:p.Ile435=
NM_001313915.1:c.1303A=	NP_001300844.1:p.Ile435=
NM_004836.5:c.1756A=	NP_004827.4:p.Ile586=
NM_004836.6:c.1756A=	NP_004827.4:p.Ile586=
XM_005264649.3:c.1072A=	XP_005264706.1:p.Ile358=
XR_939749.1:n.1965A=
XM_017005376.2:c.1072A=	XP_016860865.1:p.Ile358=
NM_004836.7:c.1756A= MANE Select	NP_004827.4:p.Ile586=
NM_001313915.2:c.1303A=	NP_001300844.1:p.Ile435=