Canonical Allele Identifier: CA1425883139
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138179G= , CM000665.2:g.184138179G= GRCh38
NC_000003.11:g.183855967G= , CM000665.1:g.183855967G= GRCh37
NC_000003.10:g.185338661G= NCBI36
NG_015826.1:g.8158G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.721G=
ENST00000468748.7:n.681G=
ENST00000484154.2:n.1319G=
ENST00000491008.6:n.1446G=
ENST00000492226.2:n.695G=
ENST00000492773.6:c.452G=
ENST00000647636.1:c.698G= ENSP00000497505.1:p.Gly233=
ENST00000647909.1:c.722G= ENSP00000498164.1:p.Gly241=
ENST00000648145.1:c.466G=
ENST00000648189.1:c.448G=
ENST00000648256.1:c.647G= ENSP00000497356.1:p.Gly216=
ENST00000648314.1:c.698G= ENSP00000496920.1:p.Gly233=
ENST00000648599.1:c.698G= ENSP00000497159.1:p.Gly233=
ENST00000648630.1:c.692G= ENSP00000497887.1:p.Gly231=
ENST00000648682.1:c.698G= ENSP00000498185.1:p.Gly233=
ENST00000648882.1:c.*524G= ENSP00000497603.1:n.*524G=
ENST00000648890.1:c.698G= ENSP00000497503.1:p.Gly233=
ENST00000648915.2:c.698G= MANE Select ENSP00000497160.1:p.Gly233=
ENST00000649545.1:c.432G=
ENST00000649688.1:c.698G= ENSP00000497097.1:p.Gly233=
ENST00000649814.1:n.747G=
ENST00000650270.1:c.565G=
ENST00000273783.7:c.698G= ENSP00000273783.3:p.Gly233=
ENST00000432982.5:c.245+1504G=
ENST00000444495.1:c.698G= ENSP00000409142.1:p.Gly233=
ENST00000468748.5:n.151G=
ENST00000479833.1:n.14G=
ENST00000481054.5:n.699G=
ENST00000491008.5:n.662G=
ENST00000491144.5:n.1138G=
NM_003907.2:c.698G= NP_003898.2:p.Gly233=
XR_924208.1:n.1649G=
NM_003907.3:c.698G= MANE Select NP_003898.2:p.Gly233=
XM_011513266.3:c.-204G= XP_011511568.1:n.-204G=
XR_001740352.2:n.1061G=
XR_001740353.2:n.1061G=
XR_924208.2:n.1061G=