Canonical Allele Identifier: CA51486342
Gene: EIF2AK3 HGNC NCBI

Linked Data

dbSNP Id: rs866676281

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575132G>A , CM000664.2:g.88575132G>A GRCh38
NC_000002.11:g.88874650G>A , CM000664.1:g.88874650G>A GRCh37
NC_000002.10:g.88655765G>A NCBI36
NG_016424.1:g.57445C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2179C>T
ENST00000682276.1:n.1796C>T
ENST00000682892.1:c.1898C>T ENSP00000507214.1:p.Ser633Phe
ENST00000682952.1:n.1990C>T
ENST00000684455.1:c.1564C>T
ENST00000684642.1:c.1748C>T ENSP00000507355.1:p.Ser583Phe
ENST00000684740.1:n.2529C>T
ENST00000303236.9:c.2351C>T MANE Select ENSP00000307235.3:p.Ser784Phe
ENST00000652099.1:c.2545C>T
ENST00000652736.1:n.2227C>T
ENST00000303236.7:c.2351C>T ENSP00000307235.3:p.Ser784Phe
ENST00000415570.1:c.1988C>T ENSP00000412076.1:p.Ser663Phe
ENST00000419748.5:c.1898C>T ENSP00000408325.1:p.Ser633Phe
ENST00000470706.1:n.49-55C>T
NM_001313915.1:c.1898C>T NP_001300844.1:p.Ser633Phe
NM_004836.5:c.2351C>T NP_004827.4:p.Ser784Phe
NM_004836.6:c.2351C>T NP_004827.4:p.Ser784Phe
NR_110236.1:n.1269G>A
XM_005264649.3:c.1667C>T XP_005264706.1:p.Ser556Phe
XM_017005376.2:c.1667C>T XP_016860865.1:p.Ser556Phe
NM_004836.7:c.2351C>T MANE Select NP_004827.4:p.Ser784Phe
NM_001313915.2:c.1898C>T NP_001300844.1:p.Ser633Phe