Canonical Allele Identifier: CA1268214701

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88590586G= , CM000664.2:g.88590586G=	GRCh38
NC_000002.11:g.88890104G= , CM000664.1:g.88890104G=	GRCh37
NC_000002.10:g.88671219G=	NCBI36
NG_016424.1:g.41991C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000681996.1:n.2213C=
ENST00000682276.1:n.477C=
ENST00000682892.1:c.569C=	ENSP00000507214.1:p.Ser190=
ENST00000682952.1:n.661C=
ENST00000684455.1:c.235C=
ENST00000684642.1:c.419C=	ENSP00000507355.1:p.Ser140=
ENST00000303236.9:c.1022C= MANE Select	ENSP00000307235.3:p.Ser341=
ENST00000652099.1:c.1216C=
ENST00000652736.1:n.898C=
ENST00000303236.7:c.1022C=	ENSP00000307235.3:p.Ser341=
ENST00000415570.1:c.659C=	ENSP00000412076.1:p.Ser220=
ENST00000419748.5:c.569C=	ENSP00000408325.1:p.Ser190=
NM_001313915.1:c.569C=	NP_001300844.1:p.Ser190=
NM_004836.5:c.1022C=	NP_004827.4:p.Ser341=
NM_004836.6:c.1022C=	NP_004827.4:p.Ser341=
XM_005264649.3:c.338C=	XP_005264706.1:p.Ser113=
XR_939749.1:n.1231C=
XM_017005376.2:c.338C=	XP_016860865.1:p.Ser113=
NM_004836.7:c.1022C= MANE Select	NP_004827.4:p.Ser341=
NM_001313915.2:c.569C=	NP_001300844.1:p.Ser190=