Canonical Allele Identifier: CA1425882851
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137908A= , CM000665.2:g.184137908A= GRCh38
NC_000003.11:g.183855696A= , CM000665.1:g.183855696A= GRCh37
NC_000003.10:g.185338390A= NCBI36
NG_015826.1:g.7887A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.540A=
ENST00000468748.7:n.500A=
ENST00000484154.2:n.1138A=
ENST00000491008.6:n.1265A=
ENST00000492226.2:n.514A=
ENST00000492773.6:c.249A=
ENST00000647636.1:c.517A= ENSP00000497505.1:p.Lys173=
ENST00000647909.1:c.541A= ENSP00000498164.1:p.Lys181=
ENST00000648145.1:c.285A=
ENST00000648189.1:c.267A=
ENST00000648256.1:c.466A= ENSP00000497356.1:p.Lys156=
ENST00000648314.1:c.517A= ENSP00000496920.1:p.Lys173=
ENST00000648599.1:c.517A= ENSP00000497159.1:p.Lys173=
ENST00000648630.1:c.511A= ENSP00000497887.1:p.Lys171=
ENST00000648682.1:c.517A= ENSP00000498185.1:p.Lys173=
ENST00000648882.1:c.*343A= ENSP00000497603.1:n.*343A=
ENST00000648890.1:c.517A= ENSP00000497503.1:p.Lys173=
ENST00000648915.2:c.517A= MANE Select ENSP00000497160.1:p.Lys173=
ENST00000649545.1:c.251A=
ENST00000649688.1:c.517A= ENSP00000497097.1:p.Lys173=
ENST00000649814.1:n.566A=
ENST00000650244.1:c.662A= ENSP00000497227.1:n.662A=
ENST00000650270.1:c.384A=
ENST00000273783.7:c.517A= ENSP00000273783.3:p.Lys173=
ENST00000432982.5:c.245+1233A=
ENST00000444495.1:c.517A= ENSP00000409142.1:p.Lys173=
ENST00000481054.5:n.518A=
ENST00000491008.5:n.481A=
ENST00000491144.5:n.957A=
ENST00000498831.1:n.472A=
NM_003907.2:c.517A= NP_003898.2:p.Lys173=
XR_924208.1:n.1468A=
NM_003907.3:c.517A= MANE Select NP_003898.2:p.Lys173=
XM_011513266.3:c.-385A= XP_011511568.1:n.-385A=
XR_001740352.2:n.880A=
XR_001740353.2:n.880A=
XR_924208.2:n.880A=