Canonical Allele Identifier: CA1425882903
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137943C= , CM000665.2:g.184137943C= GRCh38
NC_000003.11:g.183855731C= , CM000665.1:g.183855731C= GRCh37
NC_000003.10:g.185338425C= NCBI36
NG_015826.1:g.7922C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.575C=
ENST00000468748.7:n.535C=
ENST00000484154.2:n.1173C=
ENST00000491008.6:n.1300C=
ENST00000492226.2:n.549C=
ENST00000492773.6:c.284C=
ENST00000647636.1:c.552C= ENSP00000497505.1:p.Ile184=
ENST00000647909.1:c.576C= ENSP00000498164.1:p.Ile192=
ENST00000648145.1:c.320C=
ENST00000648189.1:c.302C=
ENST00000648256.1:c.501C= ENSP00000497356.1:p.Ile167=
ENST00000648314.1:c.552C= ENSP00000496920.1:p.Ile184=
ENST00000648599.1:c.552C= ENSP00000497159.1:p.Ile184=
ENST00000648630.1:c.546C= ENSP00000497887.1:p.Ile182=
ENST00000648682.1:c.552C= ENSP00000498185.1:p.Ile184=
ENST00000648882.1:c.*378C= ENSP00000497603.1:n.*378C=
ENST00000648890.1:c.552C= ENSP00000497503.1:p.Ile184=
ENST00000648915.2:c.552C= MANE Select ENSP00000497160.1:p.Ile184=
ENST00000649545.1:c.286C=
ENST00000649688.1:c.552C= ENSP00000497097.1:p.Ile184=
ENST00000649814.1:n.601C=
ENST00000650270.1:c.419C=
ENST00000273783.7:c.552C= ENSP00000273783.3:p.Ile184=
ENST00000432982.5:c.245+1268C=
ENST00000444495.1:c.552C= ENSP00000409142.1:p.Ile184=
ENST00000468748.5:n.5C=
ENST00000481054.5:n.553C=
ENST00000491008.5:n.516C=
ENST00000491144.5:n.992C=
ENST00000498831.1:n.507C=
NM_003907.2:c.552C= NP_003898.2:p.Ile184=
XR_924208.1:n.1503C=
NM_003907.3:c.552C= MANE Select NP_003898.2:p.Ile184=
XM_011513266.3:c.-350C= XP_011511568.1:n.-350C=
XR_001740352.2:n.915C=
XR_001740353.2:n.915C=
XR_924208.2:n.915C=