Canonical Allele Identifier: CA347592442
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575276C>A , CM000664.2:g.88575276C>A GRCh38
NC_000002.11:g.88874794C>A , CM000664.1:g.88874794C>A GRCh37
NC_000002.10:g.88655909C>A NCBI36
NG_016424.1:g.57301G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000478003.2:n.2035G>T
ENST00000682276.1:n.1652G>T
ENST00000682892.1:c.1754G>T ENSP00000507214.1:p.Ser585Ile
ENST00000682952.1:n.1846G>T
ENST00000684455.1:c.1420G>T
ENST00000684642.1:c.1604G>T ENSP00000507355.1:p.Ser535Ile
ENST00000684740.1:n.2385G>T
ENST00000303236.9:c.2207G>T MANE Select ENSP00000307235.3:p.Ser736Ile
ENST00000652099.1:c.2401G>T
ENST00000652736.1:n.2083G>T
ENST00000303236.7:c.2207G>T ENSP00000307235.3:p.Ser736Ile
ENST00000415570.1:c.1844G>T ENSP00000412076.1:p.Ser615Ile
ENST00000419748.5:c.1754G>T ENSP00000408325.1:p.Ser585Ile
ENST00000470706.1:n.48+85G>T
NM_001313915.1:c.1754G>T NP_001300844.1:p.Ser585Ile
NM_004836.5:c.2207G>T NP_004827.4:p.Ser736Ile
NM_004836.6:c.2207G>T NP_004827.4:p.Ser736Ile
NR_110236.1:n.1413C>A
XM_005264649.3:c.1523G>T XP_005264706.1:p.Ser508Ile
XR_939749.1:n.2486G>T
XM_017005376.2:c.1523G>T XP_016860865.1:p.Ser508Ile
NM_004836.7:c.2207G>T MANE Select NP_004827.4:p.Ser736Ile
NM_001313915.2:c.1754G>T NP_001300844.1:p.Ser585Ile