Canonical Allele Identifier: CA1268214655

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88590479C= , CM000664.2:g.88590479C=	GRCh38
NC_000002.11:g.88889997C= , CM000664.1:g.88889997C=	GRCh37
NC_000002.10:g.88671112C=	NCBI36
NG_016424.1:g.42098G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681996.1:n.2320G=
ENST00000682276.1:n.584G=
ENST00000682892.1:c.676G=	ENSP00000507214.1:p.Ala226=
ENST00000682952.1:n.768G=
ENST00000684455.1:c.342G=
ENST00000684642.1:c.526G=	ENSP00000507355.1:p.Ala176=
ENST00000303236.9:c.1129G= MANE Select	ENSP00000307235.3:p.Ala377=
ENST00000652099.1:c.1323G=
ENST00000652736.1:n.1005G=
ENST00000303236.7:c.1129G=	ENSP00000307235.3:p.Ala377=
ENST00000415570.1:c.766G=	ENSP00000412076.1:p.Ala256=
ENST00000419748.5:c.676G=	ENSP00000408325.1:p.Ala226=
NM_001313915.1:c.676G=	NP_001300844.1:p.Ala226=
NM_004836.5:c.1129G=	NP_004827.4:p.Ala377=
NM_004836.6:c.1129G=	NP_004827.4:p.Ala377=
XM_005264649.3:c.445G=	XP_005264706.1:p.Ala149=
XR_939749.1:n.1338G=
XM_017005376.2:c.445G=	XP_016860865.1:p.Ala149=
NM_004836.7:c.1129G= MANE Select	NP_004827.4:p.Ala377=
NM_001313915.2:c.676G=	NP_001300844.1:p.Ala226=