Canonical Allele Identifier: CA347591317
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575028T>A , CM000664.2:g.88575028T>A GRCh38
NC_000002.11:g.88874546T>A , CM000664.1:g.88874546T>A GRCh37
NC_000002.10:g.88655661T>A NCBI36
NG_016424.1:g.57549A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2283A>T
ENST00000682276.1:n.1900A>T
ENST00000682892.1:c.2002A>T ENSP00000507214.1:p.Lys668Ter
ENST00000682952.1:n.2094A>T
ENST00000684455.1:c.1668A>T
ENST00000684642.1:c.1852A>T ENSP00000507355.1:p.Lys618Ter
ENST00000684740.1:n.2633A>T
ENST00000303236.9:c.2455A>T MANE Select ENSP00000307235.3:p.Lys819Ter
ENST00000652099.1:c.2649A>T
ENST00000652736.1:n.2331A>T
ENST00000303236.7:c.2455A>T ENSP00000307235.3:p.Lys819Ter
ENST00000415570.1:c.2092A>T ENSP00000412076.1:p.Lys698Ter
ENST00000419748.5:c.2002A>T ENSP00000408325.1:p.Lys668Ter
ENST00000470706.1:n.98A>T
NM_001313915.1:c.2002A>T NP_001300844.1:p.Lys668Ter
NM_004836.5:c.2455A>T NP_004827.4:p.Lys819Ter
NM_004836.6:c.2455A>T NP_004827.4:p.Lys819Ter
NR_110236.1:n.1165T>A
XM_005264649.3:c.1771A>T XP_005264706.1:p.Lys591Ter
XM_017005376.2:c.1771A>T XP_016860865.1:p.Lys591Ter
NM_004836.7:c.2455A>T MANE Select NP_004827.4:p.Lys819Ter
NM_001313915.2:c.2002A>T NP_001300844.1:p.Lys668Ter