Canonical Allele Identifier: CA1425882868
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137920A= , CM000665.2:g.184137920A= GRCh38
NC_000003.11:g.183855708A= , CM000665.1:g.183855708A= GRCh37
NC_000003.10:g.185338402A= NCBI36
NG_015826.1:g.7899A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.552A=
ENST00000468748.7:n.512A=
ENST00000484154.2:n.1150A=
ENST00000491008.6:n.1277A=
ENST00000492226.2:n.526A=
ENST00000492773.6:c.261A=
ENST00000647636.1:c.529A= ENSP00000497505.1:p.Asn177=
ENST00000647909.1:c.553A= ENSP00000498164.1:p.Asn185=
ENST00000648145.1:c.297A=
ENST00000648189.1:c.279A=
ENST00000648256.1:c.478A= ENSP00000497356.1:p.Asn160=
ENST00000648314.1:c.529A= ENSP00000496920.1:p.Asn177=
ENST00000648599.1:c.529A= ENSP00000497159.1:p.Asn177=
ENST00000648630.1:c.523A= ENSP00000497887.1:p.Asn175=
ENST00000648682.1:c.529A= ENSP00000498185.1:p.Asn177=
ENST00000648882.1:c.*355A= ENSP00000497603.1:n.*355A=
ENST00000648890.1:c.529A= ENSP00000497503.1:p.Asn177=
ENST00000648915.2:c.529A= MANE Select ENSP00000497160.1:p.Asn177=
ENST00000649545.1:c.263A=
ENST00000649688.1:c.529A= ENSP00000497097.1:p.Asn177=
ENST00000649814.1:n.578A=
ENST00000650244.1:c.674A= ENSP00000497227.1:n.674A=
ENST00000650270.1:c.396A=
ENST00000273783.7:c.529A= ENSP00000273783.3:p.Asn177=
ENST00000432982.5:c.245+1245A=
ENST00000444495.1:c.529A= ENSP00000409142.1:p.Asn177=
ENST00000481054.5:n.530A=
ENST00000491008.5:n.493A=
ENST00000491144.5:n.969A=
ENST00000498831.1:n.484A=
NM_003907.2:c.529A= NP_003898.2:p.Asn177=
XR_924208.1:n.1480A=
NM_003907.3:c.529A= MANE Select NP_003898.2:p.Asn177=
XM_011513266.3:c.-373A= XP_011511568.1:n.-373A=
XR_001740352.2:n.892A=
XR_001740353.2:n.892A=
XR_924208.2:n.892A=