Canonical Allele Identifier: CA1425883169
Gene: EIF2B5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.184138206A= , CM000665.2:g.184138206A= GRCh38
NC_000003.11:g.183855994A= , CM000665.1:g.183855994A= GRCh37
NC_000003.10:g.185338688A= NCBI36
NG_015826.1:g.8185A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000465218.3:n.748A=
ENST00000468748.7:n.708A=
ENST00000484154.2:n.1346A=
ENST00000491008.6:n.1473A=
ENST00000492226.2:n.722A=
ENST00000492773.6:c.479A=
ENST00000647636.1:c.725A= ENSP00000497505.1:p.Tyr242=
ENST00000647909.1:c.749A= ENSP00000498164.1:p.Tyr250=
ENST00000648145.1:c.493A=
ENST00000648189.1:c.475A=
ENST00000648256.1:c.674A= ENSP00000497356.1:p.Tyr225=
ENST00000648314.1:c.725A= ENSP00000496920.1:p.Tyr242=
ENST00000648599.1:c.725A= ENSP00000497159.1:p.Tyr242=
ENST00000648630.1:c.719A= ENSP00000497887.1:p.Tyr240=
ENST00000648682.1:c.725A= ENSP00000498185.1:p.Tyr242=
ENST00000648882.1:c.*551A= ENSP00000497603.1:n.*551A=
ENST00000648890.1:c.725A= ENSP00000497503.1:p.Tyr242=
ENST00000648915.2:c.725A= MANE Select ENSP00000497160.1:p.Tyr242=
ENST00000649545.1:c.459A=
ENST00000649688.1:c.725A= ENSP00000497097.1:p.Tyr242=
ENST00000649814.1:n.774A=
ENST00000650270.1:c.592A=
ENST00000273783.7:c.725A= ENSP00000273783.3:p.Tyr242=
ENST00000432982.5:c.245+1531A=
ENST00000444495.1:c.725A= ENSP00000409142.1:p.Tyr242=
ENST00000468748.5:n.178A=
ENST00000479833.1:n.41A=
ENST00000481054.5:n.726A=
ENST00000491008.5:n.689A=
ENST00000491144.5:n.1165A=
NM_003907.2:c.725A= NP_003898.2:p.Tyr242=
XR_924208.1:n.1676A=
NM_003907.3:c.725A= MANE Select NP_003898.2:p.Tyr242=
XM_011513266.3:c.-177A= XP_011511568.1:n.-177A=
XR_001740352.2:n.1088A=
XR_001740353.2:n.1088A=
XR_924208.2:n.1088A=