Canonical Allele Identifier: CA1425883067

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184138088C= , CM000665.2:g.184138088C=	GRCh38
NC_000003.11:g.183855876C= , CM000665.1:g.183855876C=	GRCh37
NC_000003.10:g.185338570C=	NCBI36
NG_015826.1:g.8067C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.707+13C=
ENST00000468748.7:n.667+13C=
ENST00000484154.2:n.1305+13C=
ENST00000491008.6:n.1432+13C=
ENST00000492226.2:n.681+13C=
ENST00000492773.6:c.416+13C=
ENST00000647636.1:c.684+13C=	ENSP00000497505.1:n.684+13C=
ENST00000647909.1:c.708+13C=	ENSP00000498164.1:n.708+13C=
ENST00000648145.1:c.452+13C=
ENST00000648189.1:c.434+13C=
ENST00000648256.1:c.633+13C=	ENSP00000497356.1:n.633+13C=
ENST00000648314.1:c.684+13C=	ENSP00000496920.1:n.684+13C=
ENST00000648599.1:c.684+13C=	ENSP00000497159.1:n.684+13C=
ENST00000648630.1:c.678+13C=	ENSP00000497887.1:n.678+13C=
ENST00000648682.1:c.684+13C=	ENSP00000498185.1:n.684+13C=
ENST00000648882.1:c.*510+13C=	ENSP00000497603.1:n.*510+13C=
ENST00000648890.1:c.684+13C=	ENSP00000497503.1:n.684+13C=
ENST00000648915.2:c.684+13C= MANE Select	ENSP00000497160.1:n.684+13C=
ENST00000649545.1:c.418+13C=
ENST00000649688.1:c.684+13C=	ENSP00000497097.1:n.684+13C=
ENST00000649814.1:n.733+13C=
ENST00000650270.1:c.551+13C=
ENST00000273783.7:c.684+13C=	ENSP00000273783.3:n.684+13C=
ENST00000432982.5:c.245+1413C=
ENST00000444495.1:c.684+13C=	ENSP00000409142.1:n.684+13C=
ENST00000468748.5:n.137+13C=
ENST00000481054.5:n.685+13C=
ENST00000491008.5:n.648+13C=
ENST00000491144.5:n.1124+13C=
NM_003907.2:c.684+13C=	NP_003898.2:n.684+13C=
XR_924208.1:n.1635+13C=
NM_003907.3:c.684+13C= MANE Select	NP_003898.2:n.684+13C=
XM_011513266.3:c.-218+13C=	XP_011511568.1:n.-218+13C=
XR_001740352.2:n.1047+13C=
XR_001740353.2:n.1047+13C=
XR_924208.2:n.1047+13C=