Canonical Allele Identifier: CA355381367
Gene: EIF2B5 HGNC NCBI

Linked Data

dbSNP Id: rs1206713854

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184135556C>A , CM000665.2:g.184135556C>A GRCh38
NC_000003.11:g.183853344C>A , CM000665.1:g.183853344C>A GRCh37
NC_000003.10:g.185336038C>A NCBI36
NG_015826.1:g.5535C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000432569.2:c.171C>A ENSP00000414775.1:p.Phe57Leu
ENST00000465218.3:n.194C>A
ENST00000468748.7:n.154C>A
ENST00000471832.2:c.171C>A ENSP00000497786.1:p.Phe57Leu
ENST00000491008.6:n.36C>A
ENST00000492226.2:n.168C>A
ENST00000647636.1:c.171C>A ENSP00000497505.1:p.Phe57Leu
ENST00000647909.1:c.171C>A ENSP00000498164.1:p.Phe57Leu
ENST00000648256.1:c.120C>A ENSP00000497356.1:p.Phe40Leu
ENST00000648314.1:c.171C>A ENSP00000496920.1:p.Phe57Leu
ENST00000648599.1:c.171C>A ENSP00000497159.1:p.Phe57Leu
ENST00000648630.1:c.165C>A ENSP00000497887.1:p.Phe55Leu
ENST00000648682.1:c.171C>A ENSP00000498185.1:p.Phe57Leu
ENST00000648882.1:c.171C>A ENSP00000497603.1:p.Phe57Leu
ENST00000648890.1:c.171C>A ENSP00000497503.1:p.Phe57Leu
ENST00000648915.2:c.171C>A MANE Select ENSP00000497160.1:p.Phe57Leu
ENST00000649688.1:c.171C>A ENSP00000497097.1:p.Phe57Leu
ENST00000649814.1:n.220C>A
ENST00000650244.1:c.63C>A ENSP00000497227.1:p.Phe21Leu
ENST00000650270.1:c.38C>A
ENST00000273783.7:c.171C>A ENSP00000273783.3:p.Phe57Leu
ENST00000432569.1:c.171C>A ENSP00000414775.1:p.Phe57Leu
ENST00000432982.5:c.157C>A
ENST00000444495.1:c.171C>A ENSP00000409142.1:p.Phe57Leu
ENST00000481054.5:n.172C>A
ENST00000491144.5:n.519C>A
NM_003907.2:c.171C>A NP_003898.2:p.Phe57Leu
XR_924208.1:n.1122C>A
NM_003907.3:c.171C>A MANE Select NP_003898.2:p.Phe57Leu
XM_011513266.3:c.-731C>A XP_011511568.1:n.-731C>A
XR_001740352.2:n.534C>A
XR_001740353.2:n.534C>A
XR_924208.2:n.534C>A