Canonical Allele Identifier: CA347591754

Gene: EIF2AK3

Linked Data

• MyVariant Identifiers: chr2:g.88874644T>A (hg19) ; chr2:g.88575126T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88575126T>A , CM000664.2:g.88575126T>A	GRCh38
NC_000002.11:g.88874644T>A , CM000664.1:g.88874644T>A	GRCh37
NC_000002.10:g.88655759T>A	NCBI36
NG_016424.1:g.57451A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000478003.2:n.2185A>T
ENST00000682276.1:n.1802A>T
ENST00000682892.1:c.1904A>T	ENSP00000507214.1:p.Glu635Val
ENST00000682952.1:n.1996A>T
ENST00000684455.1:c.1570A>T
ENST00000684642.1:c.1754A>T	ENSP00000507355.1:p.Glu585Val
ENST00000684740.1:n.2535A>T
ENST00000303236.9:c.2357A>T MANE Select	ENSP00000307235.3:p.Glu786Val
ENST00000652099.1:c.2551A>T
ENST00000652736.1:n.2233A>T
ENST00000303236.7:c.2357A>T	ENSP00000307235.3:p.Glu786Val
ENST00000415570.1:c.1994A>T	ENSP00000412076.1:p.Glu665Val
ENST00000419748.5:c.1904A>T	ENSP00000408325.1:p.Glu635Val
ENST00000470706.1:n.49-49A>T
NM_001313915.1:c.1904A>T	NP_001300844.1:p.Glu635Val
NM_004836.5:c.2357A>T	NP_004827.4:p.Glu786Val
NM_004836.6:c.2357A>T	NP_004827.4:p.Glu786Val
NR_110236.1:n.1263T>A
XM_005264649.3:c.1673A>T	XP_005264706.1:p.Glu558Val
XM_017005376.2:c.1673A>T	XP_016860865.1:p.Glu558Val
NM_004836.7:c.2357A>T MANE Select	NP_004827.4:p.Glu786Val
NM_001313915.2:c.1904A>T	NP_001300844.1:p.Glu635Val