Canonical Allele Identifier: CA1425882871
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137922T= , CM000665.2:g.184137922T= GRCh38
NC_000003.11:g.183855710T= , CM000665.1:g.183855710T= GRCh37
NC_000003.10:g.185338404T= NCBI36
NG_015826.1:g.7901T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.554T=
ENST00000468748.7:n.514T=
ENST00000484154.2:n.1152T=
ENST00000491008.6:n.1279T=
ENST00000492226.2:n.528T=
ENST00000492773.6:c.263T=
ENST00000647636.1:c.531T= ENSP00000497505.1:p.Asn177=
ENST00000647909.1:c.555T= ENSP00000498164.1:p.Asn185=
ENST00000648145.1:c.299T=
ENST00000648189.1:c.281T=
ENST00000648256.1:c.480T= ENSP00000497356.1:p.Asn160=
ENST00000648314.1:c.531T= ENSP00000496920.1:p.Asn177=
ENST00000648599.1:c.531T= ENSP00000497159.1:p.Asn177=
ENST00000648630.1:c.525T= ENSP00000497887.1:p.Asn175=
ENST00000648682.1:c.531T= ENSP00000498185.1:p.Asn177=
ENST00000648882.1:c.*357T= ENSP00000497603.1:n.*357T=
ENST00000648890.1:c.531T= ENSP00000497503.1:p.Asn177=
ENST00000648915.2:c.531T= MANE Select ENSP00000497160.1:p.Asn177=
ENST00000649545.1:c.265T=
ENST00000649688.1:c.531T= ENSP00000497097.1:p.Asn177=
ENST00000649814.1:n.580T=
ENST00000650244.1:c.676T= ENSP00000497227.1:n.676T=
ENST00000650270.1:c.398T=
ENST00000273783.7:c.531T= ENSP00000273783.3:p.Asn177=
ENST00000432982.5:c.245+1247T=
ENST00000444495.1:c.531T= ENSP00000409142.1:p.Asn177=
ENST00000481054.5:n.532T=
ENST00000491008.5:n.495T=
ENST00000491144.5:n.971T=
ENST00000498831.1:n.486T=
NM_003907.2:c.531T= NP_003898.2:p.Asn177=
XR_924208.1:n.1482T=
NM_003907.3:c.531T= MANE Select NP_003898.2:p.Asn177=
XM_011513266.3:c.-371T= XP_011511568.1:n.-371T=
XR_001740352.2:n.894T=
XR_001740353.2:n.894T=
XR_924208.2:n.894T=