Canonical Allele Identifier: CA347591297
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575023T>A , CM000664.2:g.88575023T>A GRCh38
NC_000002.11:g.88874541T>A , CM000664.1:g.88874541T>A GRCh37
NC_000002.10:g.88655656T>A NCBI36
NG_016424.1:g.57554A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2288A>T
ENST00000682103.1:c.1A>T
ENST00000682276.1:n.1905A>T
ENST00000682892.1:c.2007A>T ENSP00000507214.1:p.Glu669Asp
ENST00000682952.1:n.2099A>T
ENST00000684455.1:c.1673A>T
ENST00000684642.1:c.1857A>T ENSP00000507355.1:p.Glu619Asp
ENST00000684740.1:n.2638A>T
ENST00000303236.9:c.2460A>T MANE Select ENSP00000307235.3:p.Glu820Asp
ENST00000652099.1:c.2654A>T
ENST00000652736.1:n.2336A>T
ENST00000303236.7:c.2460A>T ENSP00000307235.3:p.Glu820Asp
ENST00000415570.1:c.2097A>T ENSP00000412076.1:p.Glu699Asp
ENST00000419748.5:c.2007A>T ENSP00000408325.1:p.Glu669Asp
ENST00000470706.1:n.103A>T
NM_001313915.1:c.2007A>T NP_001300844.1:p.Glu669Asp
NM_004836.5:c.2460A>T NP_004827.4:p.Glu820Asp
NM_004836.6:c.2460A>T NP_004827.4:p.Glu820Asp
NR_110236.1:n.1160T>A
XM_005264649.3:c.1776A>T XP_005264706.1:p.Glu592Asp
XM_017005376.2:c.1776A>T XP_016860865.1:p.Glu592Asp
NM_004836.7:c.2460A>T MANE Select NP_004827.4:p.Glu820Asp
NM_001313915.2:c.2007A>T NP_001300844.1:p.Glu669Asp