Canonical Allele Identifier: CA1425883134
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138172T= , CM000665.2:g.184138172T= GRCh38
NC_000003.11:g.183855960T= , CM000665.1:g.183855960T= GRCh37
NC_000003.10:g.185338654T= NCBI36
NG_015826.1:g.8151T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.714T=
ENST00000468748.7:n.674T=
ENST00000484154.2:n.1312T=
ENST00000491008.6:n.1439T=
ENST00000492226.2:n.688T=
ENST00000492773.6:c.445T=
ENST00000647636.1:c.691T= ENSP00000497505.1:p.Phe231=
ENST00000647909.1:c.715T= ENSP00000498164.1:p.Phe239=
ENST00000648145.1:c.459T=
ENST00000648189.1:c.441T=
ENST00000648256.1:c.640T= ENSP00000497356.1:p.Phe214=
ENST00000648314.1:c.691T= ENSP00000496920.1:p.Phe231=
ENST00000648599.1:c.691T= ENSP00000497159.1:p.Phe231=
ENST00000648630.1:c.685T= ENSP00000497887.1:p.Phe229=
ENST00000648682.1:c.691T= ENSP00000498185.1:p.Phe231=
ENST00000648882.1:c.*517T= ENSP00000497603.1:n.*517T=
ENST00000648890.1:c.691T= ENSP00000497503.1:p.Phe231=
ENST00000648915.2:c.691T= MANE Select ENSP00000497160.1:p.Phe231=
ENST00000649545.1:c.425T=
ENST00000649688.1:c.691T= ENSP00000497097.1:p.Phe231=
ENST00000649814.1:n.740T=
ENST00000650270.1:c.558T=
ENST00000273783.7:c.691T= ENSP00000273783.3:p.Phe231=
ENST00000432982.5:c.245+1497T=
ENST00000444495.1:c.691T= ENSP00000409142.1:p.Phe231=
ENST00000468748.5:n.144T=
ENST00000479833.1:n.7T=
ENST00000481054.5:n.692T=
ENST00000491008.5:n.655T=
ENST00000491144.5:n.1131T=
NM_003907.2:c.691T= NP_003898.2:p.Phe231=
XR_924208.1:n.1642T=
NM_003907.3:c.691T= MANE Select NP_003898.2:p.Phe231=
XM_011513266.3:c.-211T= XP_011511568.1:n.-211T=
XR_001740352.2:n.1054T=
XR_001740353.2:n.1054T=
XR_924208.2:n.1054T=