Canonical Allele Identifier: CA1425883158
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138198G= , CM000665.2:g.184138198G= GRCh38
NC_000003.11:g.183855986G= , CM000665.1:g.183855986G= GRCh37
NC_000003.10:g.185338680G= NCBI36
NG_015826.1:g.8177G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.740G=
ENST00000468748.7:n.700G=
ENST00000484154.2:n.1338G=
ENST00000491008.6:n.1465G=
ENST00000492226.2:n.714G=
ENST00000492773.6:c.471G=
ENST00000647636.1:c.717G= ENSP00000497505.1:p.Glu239=
ENST00000647909.1:c.741G= ENSP00000498164.1:p.Glu247=
ENST00000648145.1:c.485G=
ENST00000648189.1:c.467G=
ENST00000648256.1:c.666G= ENSP00000497356.1:p.Glu222=
ENST00000648314.1:c.717G= ENSP00000496920.1:p.Glu239=
ENST00000648599.1:c.717G= ENSP00000497159.1:p.Glu239=
ENST00000648630.1:c.711G= ENSP00000497887.1:p.Glu237=
ENST00000648682.1:c.717G= ENSP00000498185.1:p.Glu239=
ENST00000648882.1:c.*543G= ENSP00000497603.1:n.*543G=
ENST00000648890.1:c.717G= ENSP00000497503.1:p.Glu239=
ENST00000648915.2:c.717G= MANE Select ENSP00000497160.1:p.Glu239=
ENST00000649545.1:c.451G=
ENST00000649688.1:c.717G= ENSP00000497097.1:p.Glu239=
ENST00000649814.1:n.766G=
ENST00000650270.1:c.584G=
ENST00000273783.7:c.717G= ENSP00000273783.3:p.Glu239=
ENST00000432982.5:c.245+1523G=
ENST00000444495.1:c.717G= ENSP00000409142.1:p.Glu239=
ENST00000468748.5:n.170G=
ENST00000479833.1:n.33G=
ENST00000481054.5:n.718G=
ENST00000491008.5:n.681G=
ENST00000491144.5:n.1157G=
NM_003907.2:c.717G= NP_003898.2:p.Glu239=
XR_924208.1:n.1668G=
NM_003907.3:c.717G= MANE Select NP_003898.2:p.Glu239=
XM_011513266.3:c.-185G= XP_011511568.1:n.-185G=
XR_001740352.2:n.1080G=
XR_001740353.2:n.1080G=
XR_924208.2:n.1080G=