Canonical Allele Identifier: CA1425883165
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138203G= , CM000665.2:g.184138203G= GRCh38
NC_000003.11:g.183855991G= , CM000665.1:g.183855991G= GRCh37
NC_000003.10:g.185338685G= NCBI36
NG_015826.1:g.8182G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.745G=
ENST00000468748.7:n.705G=
ENST00000484154.2:n.1343G=
ENST00000491008.6:n.1470G=
ENST00000492226.2:n.719G=
ENST00000492773.6:c.476G=
ENST00000647636.1:c.722G= ENSP00000497505.1:p.Arg241=
ENST00000647909.1:c.746G= ENSP00000498164.1:p.Arg249=
ENST00000648145.1:c.490G=
ENST00000648189.1:c.472G=
ENST00000648256.1:c.671G= ENSP00000497356.1:p.Arg224=
ENST00000648314.1:c.722G= ENSP00000496920.1:p.Arg241=
ENST00000648599.1:c.722G= ENSP00000497159.1:p.Arg241=
ENST00000648630.1:c.716G= ENSP00000497887.1:p.Arg239=
ENST00000648682.1:c.722G= ENSP00000498185.1:p.Arg241=
ENST00000648882.1:c.*548G= ENSP00000497603.1:n.*548G=
ENST00000648890.1:c.722G= ENSP00000497503.1:p.Arg241=
ENST00000648915.2:c.722G= MANE Select ENSP00000497160.1:p.Arg241=
ENST00000649545.1:c.456G=
ENST00000649688.1:c.722G= ENSP00000497097.1:p.Arg241=
ENST00000649814.1:n.771G=
ENST00000650270.1:c.589G=
ENST00000273783.7:c.722G= ENSP00000273783.3:p.Arg241=
ENST00000432982.5:c.245+1528G=
ENST00000444495.1:c.722G= ENSP00000409142.1:p.Arg241=
ENST00000468748.5:n.175G=
ENST00000479833.1:n.38G=
ENST00000481054.5:n.723G=
ENST00000491008.5:n.686G=
ENST00000491144.5:n.1162G=
NM_003907.2:c.722G= NP_003898.2:p.Arg241=
XR_924208.1:n.1673G=
NM_003907.3:c.722G= MANE Select NP_003898.2:p.Arg241=
XM_011513266.3:c.-180G= XP_011511568.1:n.-180G=
XR_001740352.2:n.1085G=
XR_001740353.2:n.1085G=
XR_924208.2:n.1085G=