Canonical Allele Identifier: CA347592449
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575277T>A , CM000664.2:g.88575277T>A GRCh38
NC_000002.11:g.88874795T>A , CM000664.1:g.88874795T>A GRCh37
NC_000002.10:g.88655910T>A NCBI36
NG_016424.1:g.57300A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2034A>T
ENST00000682276.1:n.1651A>T
ENST00000682892.1:c.1753A>T ENSP00000507214.1:p.Ser585Cys
ENST00000682952.1:n.1845A>T
ENST00000684455.1:c.1419A>T
ENST00000684642.1:c.1603A>T ENSP00000507355.1:p.Ser535Cys
ENST00000684740.1:n.2384A>T
ENST00000303236.9:c.2206A>T MANE Select ENSP00000307235.3:p.Ser736Cys
ENST00000652099.1:c.2400A>T
ENST00000652736.1:n.2082A>T
ENST00000303236.7:c.2206A>T ENSP00000307235.3:p.Ser736Cys
ENST00000415570.1:c.1843A>T ENSP00000412076.1:p.Ser615Cys
ENST00000419748.5:c.1753A>T ENSP00000408325.1:p.Ser585Cys
ENST00000470706.1:n.48+84A>T
NM_001313915.1:c.1753A>T NP_001300844.1:p.Ser585Cys
NM_004836.5:c.2206A>T NP_004827.4:p.Ser736Cys
NM_004836.6:c.2206A>T NP_004827.4:p.Ser736Cys
NR_110236.1:n.1414T>A
XM_005264649.3:c.1522A>T XP_005264706.1:p.Ser508Cys
XR_939749.1:n.2485A>T
XM_017005376.2:c.1522A>T XP_016860865.1:p.Ser508Cys
NM_004836.7:c.2206A>T MANE Select NP_004827.4:p.Ser736Cys
NM_001313915.2:c.1753A>T NP_001300844.1:p.Ser585Cys