Canonical Allele Identifier: CA1425882519
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137682A= , CM000665.2:g.184137682A= GRCh38
NC_000003.11:g.183855470A= , CM000665.1:g.183855470A= GRCh37
NC_000003.10:g.185338164A= NCBI36
NG_015826.1:g.7661A=

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.406A=
ENST00000468748.7:n.366A=
ENST00000484154.2:n.1004A=
ENST00000491008.6:n.1131A=
ENST00000492226.2:n.380A=
ENST00000492773.6:c.115A=
ENST00000647636.1:c.383A= ENSP00000497505.1:p.Tyr128=
ENST00000647909.1:c.383A= ENSP00000498164.1:p.Tyr128=
ENST00000648145.1:c.151A=
ENST00000648189.1:c.133A=
ENST00000648256.1:c.332A= ENSP00000497356.1:p.Tyr111=
ENST00000648314.1:c.383A= ENSP00000496920.1:p.Tyr128=
ENST00000648599.1:c.383A= ENSP00000497159.1:p.Tyr128=
ENST00000648630.1:c.377A= ENSP00000497887.1:p.Tyr126=
ENST00000648682.1:c.383A= ENSP00000498185.1:p.Tyr128=
ENST00000648882.1:c.*209A= ENSP00000497603.1:n.*209A=
ENST00000648890.1:c.383A= ENSP00000497503.1:p.Tyr128=
ENST00000648915.2:c.383A= MANE Select ENSP00000497160.1:p.Tyr128=
ENST00000649545.1:c.117A=
ENST00000649688.1:c.383A= ENSP00000497097.1:p.Tyr128=
ENST00000649814.1:n.432A=
ENST00000650244.1:c.528A= ENSP00000497227.1:n.528A=
ENST00000650270.1:c.250A=
ENST00000273783.7:c.383A= ENSP00000273783.3:p.Tyr128=
ENST00000432982.5:c.245+1007A=
ENST00000444495.1:c.383A= ENSP00000409142.1:p.Tyr128=
ENST00000481054.5:n.384A=
ENST00000491008.5:n.347A=
ENST00000491144.5:n.731A=
ENST00000498831.1:n.338A=
NM_003907.2:c.383A= NP_003898.2:p.Tyr128=
XR_924208.1:n.1334A=
NM_003907.3:c.383A= MANE Select NP_003898.2:p.Tyr128=
XM_011513266.3:c.-519A= XP_011511568.1:n.-519A=
XR_001740352.2:n.746A=
XR_001740353.2:n.746A=
XR_924208.2:n.746A=