Canonical Allele Identifier: CA1425883191
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138228C= , CM000665.2:g.184138228C= GRCh38
NC_000003.11:g.183856016C= , CM000665.1:g.183856016C= GRCh37
NC_000003.10:g.185338710C= NCBI36
NG_015826.1:g.8207C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.770C=
ENST00000468748.7:n.730C=
ENST00000484154.2:n.1368C=
ENST00000491008.6:n.1495C=
ENST00000492226.2:n.744C=
ENST00000492773.6:c.501C=
ENST00000647636.1:c.747C= ENSP00000497505.1:p.Ile249=
ENST00000647909.1:c.771C= ENSP00000498164.1:p.Ile257=
ENST00000648145.1:c.515C=
ENST00000648189.1:c.497C=
ENST00000648256.1:c.696C= ENSP00000497356.1:p.Ile232=
ENST00000648314.1:c.747C= ENSP00000496920.1:p.Ile249=
ENST00000648599.1:c.747C= ENSP00000497159.1:p.Ile249=
ENST00000648630.1:c.741C= ENSP00000497887.1:p.Ile247=
ENST00000648682.1:c.747C= ENSP00000498185.1:p.Ile249=
ENST00000648882.1:c.*573C= ENSP00000497603.1:n.*573C=
ENST00000648890.1:c.747C= ENSP00000497503.1:p.Ile249=
ENST00000648915.2:c.747C= MANE Select ENSP00000497160.1:p.Ile249=
ENST00000649545.1:c.481C=
ENST00000649688.1:c.747C= ENSP00000497097.1:p.Ile249=
ENST00000649814.1:n.796C=
ENST00000650270.1:c.614C=
ENST00000273783.7:c.747C= ENSP00000273783.3:p.Ile249=
ENST00000432982.5:c.245+1553C=
ENST00000444495.1:c.747C= ENSP00000409142.1:p.Ile249=
ENST00000468748.5:n.200C=
ENST00000479833.1:n.63C=
ENST00000481054.5:n.748C=
ENST00000491008.5:n.711C=
ENST00000491144.5:n.1187C=
NM_003907.2:c.747C= NP_003898.2:p.Ile249=
XR_924208.1:n.1698C=
NM_003907.3:c.747C= MANE Select NP_003898.2:p.Ile249=
XM_011513266.3:c.-155C= XP_011511568.1:n.-155C=
XR_001740352.2:n.1110C=
XR_001740353.2:n.1110C=
XR_924208.2:n.1110C=