Canonical Allele Identifier: CA1425883148
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138186T= , CM000665.2:g.184138186T= GRCh38
NC_000003.11:g.183855974T= , CM000665.1:g.183855974T= GRCh37
NC_000003.10:g.185338668T= NCBI36
NG_015826.1:g.8165T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.728T=
ENST00000468748.7:n.688T=
ENST00000484154.2:n.1326T=
ENST00000491008.6:n.1453T=
ENST00000492226.2:n.702T=
ENST00000492773.6:c.459T=
ENST00000647636.1:c.705T= ENSP00000497505.1:p.Ser235=
ENST00000647909.1:c.729T= ENSP00000498164.1:p.Ser243=
ENST00000648145.1:c.473T=
ENST00000648189.1:c.455T=
ENST00000648256.1:c.654T= ENSP00000497356.1:p.Ser218=
ENST00000648314.1:c.705T= ENSP00000496920.1:p.Ser235=
ENST00000648599.1:c.705T= ENSP00000497159.1:p.Ser235=
ENST00000648630.1:c.699T= ENSP00000497887.1:p.Ser233=
ENST00000648682.1:c.705T= ENSP00000498185.1:p.Ser235=
ENST00000648882.1:c.*531T= ENSP00000497603.1:n.*531T=
ENST00000648890.1:c.705T= ENSP00000497503.1:p.Ser235=
ENST00000648915.2:c.705T= MANE Select ENSP00000497160.1:p.Ser235=
ENST00000649545.1:c.439T=
ENST00000649688.1:c.705T= ENSP00000497097.1:p.Ser235=
ENST00000649814.1:n.754T=
ENST00000650270.1:c.572T=
ENST00000273783.7:c.705T= ENSP00000273783.3:p.Ser235=
ENST00000432982.5:c.245+1511T=
ENST00000444495.1:c.705T= ENSP00000409142.1:p.Ser235=
ENST00000468748.5:n.158T=
ENST00000479833.1:n.21T=
ENST00000481054.5:n.706T=
ENST00000491008.5:n.669T=
ENST00000491144.5:n.1145T=
NM_003907.2:c.705T= NP_003898.2:p.Ser235=
XR_924208.1:n.1656T=
NM_003907.3:c.705T= MANE Select NP_003898.2:p.Ser235=
XM_011513266.3:c.-197T= XP_011511568.1:n.-197T=
XR_001740352.2:n.1068T=
XR_001740353.2:n.1068T=
XR_924208.2:n.1068T=