Canonical Allele Identifier: CA1268208105
Gene: EIF2AK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575076A= , CM000664.2:g.88575076A= GRCh38
NC_000002.11:g.88874594A= , CM000664.1:g.88874594A= GRCh37
NC_000002.10:g.88655709A= NCBI36
NG_016424.1:g.57501T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2235T=
ENST00000682276.1:n.1852T=
ENST00000682892.1:c.1954T= ENSP00000507214.1:p.Ser652=
ENST00000682952.1:n.2046T=
ENST00000684455.1:c.1620T=
ENST00000684642.1:c.1804T= ENSP00000507355.1:p.Ser602=
ENST00000684740.1:n.2585T=
ENST00000303236.9:c.2407T= MANE Select ENSP00000307235.3:p.Ser803=
ENST00000652099.1:c.2601T=
ENST00000652736.1:n.2283T=
ENST00000303236.7:c.2407T= ENSP00000307235.3:p.Ser803=
ENST00000415570.1:c.2044T= ENSP00000412076.1:p.Ser682=
ENST00000419748.5:c.1954T= ENSP00000408325.1:p.Ser652=
ENST00000470706.1:n.50T=
NM_001313915.1:c.1954T= NP_001300844.1:p.Ser652=
NM_004836.5:c.2407T= NP_004827.4:p.Ser803=
NM_004836.6:c.2407T= NP_004827.4:p.Ser803=
NR_110236.1:n.1213A=
XM_005264649.3:c.1723T= XP_005264706.1:p.Ser575=
XM_017005376.2:c.1723T= XP_016860865.1:p.Ser575=
NM_004836.7:c.2407T= MANE Select NP_004827.4:p.Ser803=
NM_001313915.2:c.1954T= NP_001300844.1:p.Ser652=