Canonical Allele Identifier: CA1425879873

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184135402T= , CM000665.2:g.184135402T=	GRCh38
NC_000003.11:g.183853190T= , CM000665.1:g.183853190T=	GRCh37
NC_000003.10:g.185335884T=	NCBI36
NG_015826.1:g.5381T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.17T=	ENSP00000414775.1:p.Val6=
ENST00000465218.3:n.40T=
ENST00000471832.2:c.17T=	ENSP00000497786.1:p.Val6=
ENST00000492226.2:n.14T=
ENST00000647636.1:c.17T=	ENSP00000497505.1:p.Val6=
ENST00000647909.1:c.17T=	ENSP00000498164.1:p.Val6=
ENST00000648314.1:c.17T=	ENSP00000496920.1:p.Val6=
ENST00000648599.1:c.17T=	ENSP00000497159.1:p.Val6=
ENST00000648630.1:c.11T=	ENSP00000497887.1:p.Val4=
ENST00000648682.1:c.17T=	ENSP00000498185.1:p.Val6=
ENST00000648882.1:c.17T=	ENSP00000497603.1:p.Val6=
ENST00000648890.1:c.17T=	ENSP00000497503.1:p.Val6=
ENST00000648915.2:c.17T= MANE Select	ENSP00000497160.1:p.Val6=
ENST00000649688.1:c.17T=	ENSP00000497097.1:p.Val6=
ENST00000649814.1:n.66T=
ENST00000273783.7:c.17T=	ENSP00000273783.3:p.Val6=
ENST00000432569.1:c.17T=	ENSP00000414775.1:p.Val6=
ENST00000432982.5:c.3T=
ENST00000444495.1:c.17T=	ENSP00000409142.1:p.Val6=
ENST00000481054.5:n.18T=
ENST00000491144.5:n.365T=
NM_003907.2:c.17T=	NP_003898.2:p.Val6=
XR_924208.1:n.968T=
NM_003907.3:c.17T= MANE Select	NP_003898.2:p.Val6=
XM_011513266.3:c.-885T=	XP_011511568.1:n.-885T=
XR_001740352.2:n.380T=
XR_001740353.2:n.380T=
XR_924208.2:n.380T=