Canonical Allele Identifier: CA1268214702

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88590587A= , CM000664.2:g.88590587A=	GRCh38
NC_000002.11:g.88890105A= , CM000664.1:g.88890105A=	GRCh37
NC_000002.10:g.88671220A=	NCBI36
NG_016424.1:g.41990T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000681996.1:n.2212T=
ENST00000682276.1:n.476T=
ENST00000682892.1:c.568T=	ENSP00000507214.1:p.Ser190=
ENST00000682952.1:n.660T=
ENST00000684455.1:c.234T=
ENST00000684642.1:c.418T=	ENSP00000507355.1:p.Ser140=
ENST00000303236.9:c.1021T= MANE Select	ENSP00000307235.3:p.Ser341=
ENST00000652099.1:c.1215T=
ENST00000652736.1:n.897T=
ENST00000303236.7:c.1021T=	ENSP00000307235.3:p.Ser341=
ENST00000415570.1:c.658T=	ENSP00000412076.1:p.Ser220=
ENST00000419748.5:c.568T=	ENSP00000408325.1:p.Ser190=
NM_001313915.1:c.568T=	NP_001300844.1:p.Ser190=
NM_004836.5:c.1021T=	NP_004827.4:p.Ser341=
NM_004836.6:c.1021T=	NP_004827.4:p.Ser341=
XM_005264649.3:c.337T=	XP_005264706.1:p.Ser113=
XR_939749.1:n.1230T=
XM_017005376.2:c.337T=	XP_016860865.1:p.Ser113=
NM_004836.7:c.1021T= MANE Select	NP_004827.4:p.Ser341=
NM_001313915.2:c.568T=	NP_001300844.1:p.Ser190=