Canonical Allele Identifier: CA1425883141
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138180C= , CM000665.2:g.184138180C= GRCh38
NC_000003.11:g.183855968C= , CM000665.1:g.183855968C= GRCh37
NC_000003.10:g.185338662C= NCBI36
NG_015826.1:g.8159C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.722C=
ENST00000468748.7:n.682C=
ENST00000484154.2:n.1320C=
ENST00000491008.6:n.1447C=
ENST00000492226.2:n.696C=
ENST00000492773.6:c.453C=
ENST00000647636.1:c.699C= ENSP00000497505.1:p.Gly233=
ENST00000647909.1:c.723C= ENSP00000498164.1:p.Gly241=
ENST00000648145.1:c.467C=
ENST00000648189.1:c.449C=
ENST00000648256.1:c.648C= ENSP00000497356.1:p.Gly216=
ENST00000648314.1:c.699C= ENSP00000496920.1:p.Gly233=
ENST00000648599.1:c.699C= ENSP00000497159.1:p.Gly233=
ENST00000648630.1:c.693C= ENSP00000497887.1:p.Gly231=
ENST00000648682.1:c.699C= ENSP00000498185.1:p.Gly233=
ENST00000648882.1:c.*525C= ENSP00000497603.1:n.*525C=
ENST00000648890.1:c.699C= ENSP00000497503.1:p.Gly233=
ENST00000648915.2:c.699C= MANE Select ENSP00000497160.1:p.Gly233=
ENST00000649545.1:c.433C=
ENST00000649688.1:c.699C= ENSP00000497097.1:p.Gly233=
ENST00000649814.1:n.748C=
ENST00000650270.1:c.566C=
ENST00000273783.7:c.699C= ENSP00000273783.3:p.Gly233=
ENST00000432982.5:c.245+1505C=
ENST00000444495.1:c.699C= ENSP00000409142.1:p.Gly233=
ENST00000468748.5:n.152C=
ENST00000479833.1:n.15C=
ENST00000481054.5:n.700C=
ENST00000491008.5:n.663C=
ENST00000491144.5:n.1139C=
NM_003907.2:c.699C= NP_003898.2:p.Gly233=
XR_924208.1:n.1650C=
NM_003907.3:c.699C= MANE Select NP_003898.2:p.Gly233=
XM_011513266.3:c.-203C= XP_011511568.1:n.-203C=
XR_001740352.2:n.1062C=
XR_001740353.2:n.1062C=
XR_924208.2:n.1062C=