Canonical Allele Identifier: CA1425882423
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137636C= , CM000665.2:g.184137636C= GRCh38
NC_000003.11:g.183855424C= , CM000665.1:g.183855424C= GRCh37
NC_000003.10:g.185338118C= NCBI36
NG_015826.1:g.7615C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.360C=
ENST00000468748.7:n.320C=
ENST00000484154.2:n.958C=
ENST00000491008.6:n.1085C=
ENST00000492226.2:n.334C=
ENST00000492773.6:c.69C=
ENST00000647636.1:c.337C= ENSP00000497505.1:p.Arg113=
ENST00000647909.1:c.337C= ENSP00000498164.1:p.Arg113=
ENST00000648145.1:c.105C=
ENST00000648189.1:c.87C=
ENST00000648256.1:c.286C= ENSP00000497356.1:p.Arg96=
ENST00000648314.1:c.337C= ENSP00000496920.1:p.Arg113=
ENST00000648599.1:c.337C= ENSP00000497159.1:p.Arg113=
ENST00000648630.1:c.331C= ENSP00000497887.1:p.Arg111=
ENST00000648682.1:c.337C= ENSP00000498185.1:p.Arg113=
ENST00000648882.1:c.*163C= ENSP00000497603.1:n.*163C=
ENST00000648890.1:c.337C= ENSP00000497503.1:p.Arg113=
ENST00000648915.2:c.337C= MANE Select ENSP00000497160.1:p.Arg113=
ENST00000649545.1:c.71C=
ENST00000649688.1:c.337C= ENSP00000497097.1:p.Arg113=
ENST00000649814.1:n.386C=
ENST00000650244.1:c.482C= ENSP00000497227.1:n.482C=
ENST00000650270.1:c.204C=
ENST00000273783.7:c.337C= ENSP00000273783.3:p.Arg113=
ENST00000432982.5:c.245+961C=
ENST00000444495.1:c.337C= ENSP00000409142.1:p.Arg113=
ENST00000481054.5:n.338C=
ENST00000491008.5:n.301C=
ENST00000491144.5:n.685C=
ENST00000498831.1:n.292C=
NM_003907.2:c.337C= NP_003898.2:p.Arg113=
XR_924208.1:n.1288C=
NM_003907.3:c.337C= MANE Select NP_003898.2:p.Arg113=
XM_011513266.3:c.-565C= XP_011511568.1:n.-565C=
XR_001740352.2:n.700C=
XR_001740353.2:n.700C=
XR_924208.2:n.700C=