Canonical Allele Identifier: CA1425885543
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184140413T= , CM000665.2:g.184140413T= GRCh38
NC_000003.11:g.183858201T= , CM000665.1:g.183858201T= GRCh37
NC_000003.10:g.185340895T= NCBI36
NG_015826.1:g.10392T=

Transcript Alleles

HGVS Amino-acid change
ENST00000465218.3:n.867-5T=
ENST00000468748.7:n.1082T=
ENST00000484154.2:n.1387-1512T=
ENST00000491008.6:n.1592-5T=
ENST00000492226.2:n.1096T=
ENST00000492773.6:c.598-5T=
ENST00000647636.1:c.844-5T= ENSP00000497505.1:n.844-5T=
ENST00000647909.1:c.868-5T= ENSP00000498164.1:n.868-5T=
ENST00000648145.1:c.612-5T=
ENST00000648189.1:c.658-5T=
ENST00000648256.1:c.816-5T= ENSP00000497356.1:n.816-5T=
ENST00000648314.1:c.908-5T= ENSP00000496920.1:n.908-5T=
ENST00000648599.1:c.*127-5T= ENSP00000497159.1:n.*127-5T=
ENST00000648630.1:c.838-5T= ENSP00000497887.1:n.838-5T=
ENST00000648682.1:c.844-5T= ENSP00000498185.1:n.844-5T=
ENST00000648882.1:c.*670-5T= ENSP00000497603.1:n.*670-5T=
ENST00000648890.1:c.844-5T= ENSP00000497503.1:n.844-5T=
ENST00000648915.2:c.844-5T= MANE Select ENSP00000497160.1:n.844-5T=
ENST00000649545.1:c.577+256T=
ENST00000649688.1:c.*127-5T= ENSP00000497097.1:n.*127-5T=
ENST00000649814.1:n.893-5T=
ENST00000650270.1:c.711-5T=
ENST00000273783.7:c.844-5T= ENSP00000273783.3:n.844-5T=
ENST00000432982.5:c.246-1824T=
ENST00000444495.1:c.844-5T= ENSP00000409142.1:n.844-5T=
ENST00000468748.5:n.552T=
ENST00000479833.1:n.160-5T=
ENST00000481054.5:n.938-5T=
ENST00000491144.5:n.1348-5T=
ENST00000493740.1:n.74-5T=
NM_003907.2:c.844-5T= NP_003898.2:n.844-5T=
XM_011513265.1:c.94-5T= XP_011511567.1:n.94-5T=
XM_011513266.1:c.7-5T= XP_011511568.1:n.7-5T=
XR_924208.1:n.1795-5T=
NM_003907.3:c.844-5T= MANE Select NP_003898.2:n.844-5T=
XM_011513266.3:c.7-5T= XP_011511568.1:n.7-5T=
XR_001740352.2:n.1207-5T=
XR_001740353.2:n.1207-5T=
XR_924208.2:n.1207-5T=