Canonical Allele Identifier: CA1425883149
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138188A= , CM000665.2:g.184138188A= GRCh38
NC_000003.11:g.183855976A= , CM000665.1:g.183855976A= GRCh37
NC_000003.10:g.185338670A= NCBI36
NG_015826.1:g.8167A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.730A=
ENST00000468748.7:n.690A=
ENST00000484154.2:n.1328A=
ENST00000491008.6:n.1455A=
ENST00000492226.2:n.704A=
ENST00000492773.6:c.461A=
ENST00000647636.1:c.707A= ENSP00000497505.1:p.Asp236=
ENST00000647909.1:c.731A= ENSP00000498164.1:p.Asp244=
ENST00000648145.1:c.475A=
ENST00000648189.1:c.457A=
ENST00000648256.1:c.656A= ENSP00000497356.1:p.Asp219=
ENST00000648314.1:c.707A= ENSP00000496920.1:p.Asp236=
ENST00000648599.1:c.707A= ENSP00000497159.1:p.Asp236=
ENST00000648630.1:c.701A= ENSP00000497887.1:p.Asp234=
ENST00000648682.1:c.707A= ENSP00000498185.1:p.Asp236=
ENST00000648882.1:c.*533A= ENSP00000497603.1:n.*533A=
ENST00000648890.1:c.707A= ENSP00000497503.1:p.Asp236=
ENST00000648915.2:c.707A= MANE Select ENSP00000497160.1:p.Asp236=
ENST00000649545.1:c.441A=
ENST00000649688.1:c.707A= ENSP00000497097.1:p.Asp236=
ENST00000649814.1:n.756A=
ENST00000650270.1:c.574A=
ENST00000273783.7:c.707A= ENSP00000273783.3:p.Asp236=
ENST00000432982.5:c.245+1513A=
ENST00000444495.1:c.707A= ENSP00000409142.1:p.Asp236=
ENST00000468748.5:n.160A=
ENST00000479833.1:n.23A=
ENST00000481054.5:n.708A=
ENST00000491008.5:n.671A=
ENST00000491144.5:n.1147A=
NM_003907.2:c.707A= NP_003898.2:p.Asp236=
XR_924208.1:n.1658A=
NM_003907.3:c.707A= MANE Select NP_003898.2:p.Asp236=
XM_011513266.3:c.-195A= XP_011511568.1:n.-195A=
XR_001740352.2:n.1070A=
XR_001740353.2:n.1070A=
XR_924208.2:n.1070A=