Canonical Allele Identifier: CA1425882749
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184137812A= , CM000665.2:g.184137812A= GRCh38
NC_000003.11:g.183855600A= , CM000665.1:g.183855600A= GRCh37
NC_000003.10:g.185338294A= NCBI36
NG_015826.1:g.7791A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.529+7A=
ENST00000468748.7:n.489+7A=
ENST00000484154.2:n.1127+7A=
ENST00000491008.6:n.1254+7A=
ENST00000492226.2:n.503+7A=
ENST00000492773.6:c.238+7A=
ENST00000647636.1:c.506+7A= ENSP00000497505.1:n.506+7A=
ENST00000647909.1:c.506+7A= ENSP00000498164.1:n.506+7A=
ENST00000648145.1:c.274+7A=
ENST00000648189.1:c.256+7A=
ENST00000648256.1:c.455+7A= ENSP00000497356.1:n.455+7A=
ENST00000648314.1:c.506+7A= ENSP00000496920.1:n.506+7A=
ENST00000648599.1:c.506+7A= ENSP00000497159.1:n.506+7A=
ENST00000648630.1:c.500+7A= ENSP00000497887.1:n.500+7A=
ENST00000648682.1:c.506+7A= ENSP00000498185.1:n.506+7A=
ENST00000648882.1:c.*332+7A= ENSP00000497603.1:n.*332+7A=
ENST00000648890.1:c.506+7A= ENSP00000497503.1:n.506+7A=
ENST00000648915.2:c.506+7A= MANE Select ENSP00000497160.1:n.506+7A=
ENST00000649545.1:c.240+7A=
ENST00000649688.1:c.506+7A= ENSP00000497097.1:n.506+7A=
ENST00000649814.1:n.555+7A=
ENST00000650244.1:c.651+7A= ENSP00000497227.1:n.651+7A=
ENST00000650270.1:c.373+7A=
ENST00000273783.7:c.506+7A= ENSP00000273783.3:n.506+7A=
ENST00000432982.5:c.245+1137A=
ENST00000444495.1:c.506+7A= ENSP00000409142.1:n.506+7A=
ENST00000481054.5:n.507+7A=
ENST00000491008.5:n.470+7A=
ENST00000491144.5:n.861A=
ENST00000498831.1:n.461+7A=
NM_003907.2:c.506+7A= NP_003898.2:n.506+7A=
XR_924208.1:n.1457+7A=
NM_003907.3:c.506+7A= MANE Select NP_003898.2:n.506+7A=
XM_011513266.3:c.-396+7A= XP_011511568.1:n.-396+7A=
XR_001740352.2:n.869+7A=
XR_001740353.2:n.869+7A=
XR_924208.2:n.869+7A=