Canonical Allele Identifier: CA1425882922
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137969C= , CM000665.2:g.184137969C= GRCh38
NC_000003.11:g.183855757C= , CM000665.1:g.183855757C= GRCh37
NC_000003.10:g.185338451C= NCBI36
NG_015826.1:g.7948C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.601C=
ENST00000468748.7:n.561C=
ENST00000484154.2:n.1199C=
ENST00000491008.6:n.1326C=
ENST00000492226.2:n.575C=
ENST00000492773.6:c.310C=
ENST00000647636.1:c.578C= ENSP00000497505.1:p.Pro193=
ENST00000647909.1:c.602C= ENSP00000498164.1:p.Pro201=
ENST00000648145.1:c.346C=
ENST00000648189.1:c.328C=
ENST00000648256.1:c.527C= ENSP00000497356.1:p.Pro176=
ENST00000648314.1:c.578C= ENSP00000496920.1:p.Pro193=
ENST00000648599.1:c.578C= ENSP00000497159.1:p.Pro193=
ENST00000648630.1:c.572C= ENSP00000497887.1:p.Pro191=
ENST00000648682.1:c.578C= ENSP00000498185.1:p.Pro193=
ENST00000648882.1:c.*404C= ENSP00000497603.1:n.*404C=
ENST00000648890.1:c.578C= ENSP00000497503.1:p.Pro193=
ENST00000648915.2:c.578C= MANE Select ENSP00000497160.1:p.Pro193=
ENST00000649545.1:c.312C=
ENST00000649688.1:c.578C= ENSP00000497097.1:p.Pro193=
ENST00000649814.1:n.627C=
ENST00000650270.1:c.445C=
ENST00000273783.7:c.578C= ENSP00000273783.3:p.Pro193=
ENST00000432982.5:c.245+1294C=
ENST00000444495.1:c.578C= ENSP00000409142.1:p.Pro193=
ENST00000468748.5:n.31C=
ENST00000481054.5:n.579C=
ENST00000491008.5:n.542C=
ENST00000491144.5:n.1018C=
ENST00000498831.1:n.533C=
NM_003907.2:c.578C= NP_003898.2:p.Pro193=
XR_924208.1:n.1529C=
NM_003907.3:c.578C= MANE Select NP_003898.2:p.Pro193=
XM_011513266.3:c.-324C= XP_011511568.1:n.-324C=
XR_001740352.2:n.941C=
XR_001740353.2:n.941C=
XR_924208.2:n.941C=