Canonical Allele Identifier: CA1268208235

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575419G= , CM000664.2:g.88575419G=	GRCh38
NC_000002.11:g.88874937G= , CM000664.1:g.88874937G=	GRCh37
NC_000002.10:g.88656052G=	NCBI36
NG_016424.1:g.57158C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.1892C=
ENST00000682276.1:n.1509C=
ENST00000682892.1:c.1611C=	ENSP00000507214.1:p.Ser537=
ENST00000682952.1:n.1703C=
ENST00000684455.1:c.1277C=
ENST00000684642.1:c.1461C=	ENSP00000507355.1:p.Ser487=
ENST00000684740.1:n.2242C=
ENST00000303236.9:c.2064C= MANE Select	ENSP00000307235.3:p.Ser688=
ENST00000652099.1:c.2258C=
ENST00000652736.1:n.1940C=
ENST00000303236.7:c.2064C=	ENSP00000307235.3:p.Ser688=
ENST00000415570.1:c.1701C=	ENSP00000412076.1:p.Ser567=
ENST00000419748.5:c.1611C=	ENSP00000408325.1:p.Ser537=
ENST00000478003.1:n.630C=
NM_001313915.1:c.1611C=	NP_001300844.1:p.Ser537=
NM_004836.5:c.2064C=	NP_004827.4:p.Ser688=
NM_004836.6:c.2064C=	NP_004827.4:p.Ser688=
NR_110236.1:n.1556G=
XM_005264649.3:c.1380C=	XP_005264706.1:p.Ser460=
XR_939749.1:n.2343C=
XM_017005376.2:c.1380C=	XP_016860865.1:p.Ser460=
NM_004836.7:c.2064C= MANE Select	NP_004827.4:p.Ser688=
NM_001313915.2:c.1611C=	NP_001300844.1:p.Ser537=