Canonical Allele Identifier: CA1268211592

Gene: EIF2AK3

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88583439T= , CM000664.2:g.88583439T=	GRCh38
NC_000002.11:g.88882957T= , CM000664.1:g.88882957T=	GRCh37
NC_000002.10:g.88664072T=	NCBI36
NG_016424.1:g.49138A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682276.1:n.1199A=
ENST00000682892.1:c.1301A=	ENSP00000507214.1:p.Tyr434=
ENST00000682952.1:n.1393A=
ENST00000684455.1:c.967A=
ENST00000684642.1:c.1151A=	ENSP00000507355.1:p.Tyr384=
ENST00000303236.9:c.1754A= MANE Select	ENSP00000307235.3:p.Tyr585=
ENST00000652099.1:c.1948A=
ENST00000652736.1:n.1630A=
ENST00000303236.7:c.1754A=	ENSP00000307235.3:p.Tyr585=
ENST00000415570.1:c.1391A=	ENSP00000412076.1:p.Tyr464=
ENST00000419748.5:c.1301A=	ENSP00000408325.1:p.Tyr434=
NM_001313915.1:c.1301A=	NP_001300844.1:p.Tyr434=
NM_004836.5:c.1754A=	NP_004827.4:p.Tyr585=
NM_004836.6:c.1754A=	NP_004827.4:p.Tyr585=
XM_005264649.3:c.1070A=	XP_005264706.1:p.Tyr357=
XR_939749.1:n.1963A=
XM_017005376.2:c.1070A=	XP_016860865.1:p.Tyr357=
NM_004836.7:c.1754A= MANE Select	NP_004827.4:p.Tyr585=
NM_001313915.2:c.1301A=	NP_001300844.1:p.Tyr434=