Canonical Allele Identifier: CA1425887275
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184142057T= , CM000665.2:g.184142057T= GRCh38
NC_000003.11:g.183859845T= , CM000665.1:g.183859845T= GRCh37
NC_000003.10:g.185342539T= NCBI36
NG_015826.1:g.12036T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.1312T=
ENST00000468748.7:n.1532T=
ENST00000484154.2:n.1519T=
ENST00000491008.6:n.2037T=
ENST00000492226.2:n.1556T=
ENST00000492773.6:c.1043T=
ENST00000647636.1:c.*138T= ENSP00000497505.1:n.*138T=
ENST00000647909.1:c.1313T= ENSP00000498164.1:p.Val438=
ENST00000648145.1:c.1061T=
ENST00000648189.1:c.1107T=
ENST00000648256.1:c.1261T= ENSP00000497356.1:n.1261T=
ENST00000648314.1:c.*408T= ENSP00000496920.1:n.*408T=
ENST00000648599.1:c.*572T= ENSP00000497159.1:n.*572T=
ENST00000648630.1:c.1168T= ENSP00000497887.1:n.1168T=
ENST00000648682.1:c.*129T= ENSP00000498185.1:n.*129T=
ENST00000648882.1:c.*1115T= ENSP00000497603.1:n.*1115T=
ENST00000648890.1:c.1289T= ENSP00000497503.1:p.Val430=
ENST00000648915.2:c.1289T= MANE Select ENSP00000497160.1:p.Val430=
ENST00000649545.1:c.710T=
ENST00000649688.1:c.*582T= ENSP00000497097.1:n.*582T=
ENST00000649814.1:n.1338T=
ENST00000650270.1:c.1156T=
ENST00000273783.7:c.1289T= ENSP00000273783.3:p.Val430=
ENST00000432982.5:c.246-180T=
ENST00000444495.1:c.1289T= ENSP00000409142.1:p.Val430=
ENST00000481054.5:n.1383T=
ENST00000491144.5:n.1793T=
ENST00000492773.5:n.172T=
NM_003907.2:c.1289T= NP_003898.2:p.Val430=
XM_011513265.1:c.539T= XP_011511567.1:p.Val180=
XM_011513266.1:c.452T= XP_011511568.1:p.Val151=
XR_924208.1:n.2240T=
NM_003907.3:c.1289T= MANE Select NP_003898.2:p.Val430=
XM_011513266.3:c.452T= XP_011511568.1:p.Val151=
XR_001740352.2:n.1652T=
XR_001740353.2:n.1652T=
XR_924208.2:n.1652T=