Canonical Allele Identifier: CA347592555
Gene: EIF2AK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88575300C>G , CM000664.2:g.88575300C>G GRCh38
NC_000002.11:g.88874818C>G , CM000664.1:g.88874818C>G GRCh37
NC_000002.10:g.88655933C>G NCBI36
NG_016424.1:g.57277G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000478003.2:n.2011G>C
ENST00000682276.1:n.1628G>C
ENST00000682892.1:c.1730G>C ENSP00000507214.1:p.Cys577Ser
ENST00000682952.1:n.1822G>C
ENST00000684455.1:c.1396G>C
ENST00000684642.1:c.1580G>C ENSP00000507355.1:p.Cys527Ser
ENST00000684740.1:n.2361G>C
ENST00000303236.9:c.2183G>C MANE Select ENSP00000307235.3:p.Cys728Ser
ENST00000652099.1:c.2377G>C
ENST00000652736.1:n.2059G>C
ENST00000303236.7:c.2183G>C ENSP00000307235.3:p.Cys728Ser
ENST00000415570.1:c.1820G>C ENSP00000412076.1:p.Cys607Ser
ENST00000419748.5:c.1730G>C ENSP00000408325.1:p.Cys577Ser
ENST00000470706.1:n.48+61G>C
NM_001313915.1:c.1730G>C NP_001300844.1:p.Cys577Ser
NM_004836.5:c.2183G>C NP_004827.4:p.Cys728Ser
NM_004836.6:c.2183G>C NP_004827.4:p.Cys728Ser
NR_110236.1:n.1437C>G
XM_005264649.3:c.1499G>C XP_005264706.1:p.Cys500Ser
XR_939749.1:n.2462G>C
XM_017005376.2:c.1499G>C XP_016860865.1:p.Cys500Ser
NM_004836.7:c.2183G>C MANE Select NP_004827.4:p.Cys728Ser
NM_001313915.2:c.1730G>C NP_001300844.1:p.Cys577Ser