Canonical Allele Identifier: CA1425882949
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137985A= , CM000665.2:g.184137985A= GRCh38
NC_000003.11:g.183855773A= , CM000665.1:g.183855773A= GRCh37
NC_000003.10:g.185338467A= NCBI36
NG_015826.1:g.7964A=

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.617A=
ENST00000468748.7:n.577A=
ENST00000484154.2:n.1215A=
ENST00000491008.6:n.1342A=
ENST00000492226.2:n.591A=
ENST00000492773.6:c.326A=
ENST00000647636.1:c.594A= ENSP00000497505.1:p.Glu198=
ENST00000647909.1:c.618A= ENSP00000498164.1:p.Glu206=
ENST00000648145.1:c.362A=
ENST00000648189.1:c.344A=
ENST00000648256.1:c.543A= ENSP00000497356.1:p.Glu181=
ENST00000648314.1:c.594A= ENSP00000496920.1:p.Glu198=
ENST00000648599.1:c.594A= ENSP00000497159.1:p.Glu198=
ENST00000648630.1:c.588A= ENSP00000497887.1:p.Glu196=
ENST00000648682.1:c.594A= ENSP00000498185.1:p.Glu198=
ENST00000648882.1:c.*420A= ENSP00000497603.1:n.*420A=
ENST00000648890.1:c.594A= ENSP00000497503.1:p.Glu198=
ENST00000648915.2:c.594A= MANE Select ENSP00000497160.1:p.Glu198=
ENST00000649545.1:c.328A=
ENST00000649688.1:c.594A= ENSP00000497097.1:p.Glu198=
ENST00000649814.1:n.643A=
ENST00000650270.1:c.461A=
ENST00000273783.7:c.594A= ENSP00000273783.3:p.Glu198=
ENST00000432982.5:c.245+1310A=
ENST00000444495.1:c.594A= ENSP00000409142.1:p.Glu198=
ENST00000468748.5:n.47A=
ENST00000481054.5:n.595A=
ENST00000491008.5:n.558A=
ENST00000491144.5:n.1034A=
ENST00000498831.1:n.549A=
NM_003907.2:c.594A= NP_003898.2:p.Glu198=
XR_924208.1:n.1545A=
NM_003907.3:c.594A= MANE Select NP_003898.2:p.Glu198=
XM_011513266.3:c.-308A= XP_011511568.1:n.-308A=
XR_001740352.2:n.957A=
XR_001740353.2:n.957A=
XR_924208.2:n.957A=