Canonical Allele Identifier: CA347592039
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575193T>A , CM000664.2:g.88575193T>A GRCh38
NC_000002.11:g.88874711T>A , CM000664.1:g.88874711T>A GRCh37
NC_000002.10:g.88655826T>A NCBI36
NG_016424.1:g.57384A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2118A>T
ENST00000682276.1:n.1735A>T
ENST00000682892.1:c.1837A>T ENSP00000507214.1:p.Ser613Cys
ENST00000682952.1:n.1929A>T
ENST00000684455.1:c.1503A>T
ENST00000684642.1:c.1687A>T ENSP00000507355.1:p.Ser563Cys
ENST00000684740.1:n.2468A>T
ENST00000303236.9:c.2290A>T MANE Select ENSP00000307235.3:p.Ser764Cys
ENST00000652099.1:c.2484A>T
ENST00000652736.1:n.2166A>T
ENST00000303236.7:c.2290A>T ENSP00000307235.3:p.Ser764Cys
ENST00000415570.1:c.1927A>T ENSP00000412076.1:p.Ser643Cys
ENST00000419748.5:c.1837A>T ENSP00000408325.1:p.Ser613Cys
ENST00000470706.1:n.49-116A>T
NM_001313915.1:c.1837A>T NP_001300844.1:p.Ser613Cys
NM_004836.5:c.2290A>T NP_004827.4:p.Ser764Cys
NM_004836.6:c.2290A>T NP_004827.4:p.Ser764Cys
NR_110236.1:n.1330T>A
XM_005264649.3:c.1606A>T XP_005264706.1:p.Ser536Cys
XM_017005376.2:c.1606A>T XP_016860865.1:p.Ser536Cys
NM_004836.7:c.2290A>T MANE Select NP_004827.4:p.Ser764Cys
NM_001313915.2:c.1837A>T NP_001300844.1:p.Ser613Cys