Canonical Allele Identifier: CA1268208181
Gene: EIF2AK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575301A= , CM000664.2:g.88575301A= GRCh38
NC_000002.11:g.88874819A= , CM000664.1:g.88874819A= GRCh37
NC_000002.10:g.88655934A= NCBI36
NG_016424.1:g.57276T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000478003.2:n.2010T=
ENST00000682276.1:n.1627T=
ENST00000682892.1:c.1729T= ENSP00000507214.1:p.Cys577=
ENST00000682952.1:n.1821T=
ENST00000684455.1:c.1395T=
ENST00000684642.1:c.1579T= ENSP00000507355.1:p.Cys527=
ENST00000684740.1:n.2360T=
ENST00000303236.9:c.2182T= MANE Select ENSP00000307235.3:p.Cys728=
ENST00000652099.1:c.2376T=
ENST00000652736.1:n.2058T=
ENST00000303236.7:c.2182T= ENSP00000307235.3:p.Cys728=
ENST00000415570.1:c.1819T= ENSP00000412076.1:p.Cys607=
ENST00000419748.5:c.1729T= ENSP00000408325.1:p.Cys577=
ENST00000470706.1:n.48+60T=
NM_001313915.1:c.1729T= NP_001300844.1:p.Cys577=
NM_004836.5:c.2182T= NP_004827.4:p.Cys728=
NM_004836.6:c.2182T= NP_004827.4:p.Cys728=
NR_110236.1:n.1438A=
XM_005264649.3:c.1498T= XP_005264706.1:p.Cys500=
XR_939749.1:n.2461T=
XM_017005376.2:c.1498T= XP_016860865.1:p.Cys500=
NM_004836.7:c.2182T= MANE Select NP_004827.4:p.Cys728=
NM_001313915.2:c.1729T= NP_001300844.1:p.Cys577=