Canonical Allele Identifier: CA1425882535
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137690C= , CM000665.2:g.184137690C= GRCh38
NC_000003.11:g.183855478C= , CM000665.1:g.183855478C= GRCh37
NC_000003.10:g.185338172C= NCBI36
NG_015826.1:g.7669C=

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.414C=
ENST00000468748.7:n.374C=
ENST00000484154.2:n.1012C=
ENST00000491008.6:n.1139C=
ENST00000492226.2:n.388C=
ENST00000492773.6:c.123C=
ENST00000647636.1:c.391C= ENSP00000497505.1:p.Leu131=
ENST00000647909.1:c.391C= ENSP00000498164.1:p.Leu131=
ENST00000648145.1:c.159C=
ENST00000648189.1:c.141C=
ENST00000648256.1:c.340C= ENSP00000497356.1:p.Leu114=
ENST00000648314.1:c.391C= ENSP00000496920.1:p.Leu131=
ENST00000648599.1:c.391C= ENSP00000497159.1:p.Leu131=
ENST00000648630.1:c.385C= ENSP00000497887.1:p.Leu129=
ENST00000648682.1:c.391C= ENSP00000498185.1:p.Leu131=
ENST00000648882.1:c.*217C= ENSP00000497603.1:n.*217C=
ENST00000648890.1:c.391C= ENSP00000497503.1:p.Leu131=
ENST00000648915.2:c.391C= MANE Select ENSP00000497160.1:p.Leu131=
ENST00000649545.1:c.125C=
ENST00000649688.1:c.391C= ENSP00000497097.1:p.Leu131=
ENST00000649814.1:n.440C=
ENST00000650244.1:c.536C= ENSP00000497227.1:n.536C=
ENST00000650270.1:c.258C=
ENST00000273783.7:c.391C= ENSP00000273783.3:p.Leu131=
ENST00000432982.5:c.245+1015C=
ENST00000444495.1:c.391C= ENSP00000409142.1:p.Leu131=
ENST00000481054.5:n.392C=
ENST00000491008.5:n.355C=
ENST00000491144.5:n.739C=
ENST00000498831.1:n.346C=
NM_003907.2:c.391C= NP_003898.2:p.Leu131=
XR_924208.1:n.1342C=
NM_003907.3:c.391C= MANE Select NP_003898.2:p.Leu131=
XM_011513266.3:c.-511C= XP_011511568.1:n.-511C=
XR_001740352.2:n.754C=
XR_001740353.2:n.754C=
XR_924208.2:n.754C=