Canonical Allele Identifier: CA1425881534
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184136703G= , CM000665.2:g.184136703G= GRCh38
NC_000003.11:g.183854491G= , CM000665.1:g.183854491G= GRCh37
NC_000003.10:g.185337185G= NCBI36
NG_015826.1:g.6682G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000432569.2:c.287G= ENSP00000414775.1:p.Cys96=
ENST00000465218.3:n.310G=
ENST00000468748.7:n.270G=
ENST00000471832.2:c.*281G= ENSP00000497786.1:n.*281G=
ENST00000484154.2:n.25G=
ENST00000491008.6:n.152G=
ENST00000492226.2:n.284G=
ENST00000492773.6:c.19G=
ENST00000647636.1:c.287G= ENSP00000497505.1:p.Cys96=
ENST00000647909.1:c.287G= ENSP00000498164.1:p.Cys96=
ENST00000648145.1:c.55G=
ENST00000648189.1:c.37G=
ENST00000648256.1:c.236G= ENSP00000497356.1:p.Cys79=
ENST00000648314.1:c.287G= ENSP00000496920.1:p.Cys96=
ENST00000648599.1:c.287G= ENSP00000497159.1:p.Cys96=
ENST00000648630.1:c.281G= ENSP00000497887.1:p.Cys94=
ENST00000648682.1:c.287G= ENSP00000498185.1:p.Cys96=
ENST00000648882.1:c.*113G= ENSP00000497603.1:n.*113G=
ENST00000648890.1:c.287G= ENSP00000497503.1:p.Cys96=
ENST00000648915.2:c.287G= MANE Select ENSP00000497160.1:p.Cys96=
ENST00000649545.1:c.21G=
ENST00000649688.1:c.287G= ENSP00000497097.1:p.Cys96=
ENST00000649814.1:n.336G=
ENST00000650244.1:c.432G= ENSP00000497227.1:n.432G=
ENST00000650270.1:c.154G=
ENST00000273783.7:c.287G= ENSP00000273783.3:p.Cys96=
ENST00000432569.1:c.287G= ENSP00000414775.1:p.Cys96=
ENST00000432982.5:c.245+28G=
ENST00000444495.1:c.287G= ENSP00000409142.1:p.Cys96=
ENST00000471832.1:n.218G=
ENST00000481054.5:n.288G=
ENST00000491144.5:n.635G=
ENST00000498831.1:n.143G=
NM_003907.2:c.287G= NP_003898.2:p.Cys96=
XR_924208.1:n.1238G=
NM_003907.3:c.287G= MANE Select NP_003898.2:p.Cys96=
XM_011513266.3:c.-615G= XP_011511568.1:n.-615G=
XR_001740352.2:n.650G=
XR_001740353.2:n.650G=
XR_924208.2:n.650G=