Canonical Allele Identifier: CA1425881387

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184136583C= , CM000665.2:g.184136583C=	GRCh38
NC_000003.11:g.183854371C= , CM000665.1:g.183854371C=	GRCh37
NC_000003.10:g.185337065C=	NCBI36
NG_015826.1:g.6562C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000432569.2:c.196-29C=	ENSP00000414775.1:n.196-29C=
ENST00000465218.3:n.219-29C=
ENST00000468748.7:n.179-29C=
ENST00000471832.2:c.*190-29C=	ENSP00000497786.1:n.*190-29C=
ENST00000491008.6:n.61-29C=
ENST00000492226.2:n.193-29C=
ENST00000647636.1:c.196-29C=	ENSP00000497505.1:n.196-29C=
ENST00000647909.1:c.196-29C=	ENSP00000498164.1:n.196-29C=
ENST00000648256.1:c.145-29C=	ENSP00000497356.1:n.145-29C=
ENST00000648314.1:c.196-29C=	ENSP00000496920.1:n.196-29C=
ENST00000648599.1:c.196-29C=	ENSP00000497159.1:n.196-29C=
ENST00000648630.1:c.190-29C=	ENSP00000497887.1:n.190-29C=
ENST00000648682.1:c.196-29C=	ENSP00000498185.1:n.196-29C=
ENST00000648882.1:c.*22-29C=	ENSP00000497603.1:n.*22-29C=
ENST00000648890.1:c.196-29C=	ENSP00000497503.1:n.196-29C=
ENST00000648915.2:c.196-29C= MANE Select	ENSP00000497160.1:n.196-29C=
ENST00000649688.1:c.196-29C=	ENSP00000497097.1:n.196-29C=
ENST00000649814.1:n.245-29C=
ENST00000650244.1:c.341-29C=	ENSP00000497227.1:n.341-29C=
ENST00000650270.1:c.63-29C=
ENST00000273783.7:c.196-29C=	ENSP00000273783.3:n.196-29C=
ENST00000432569.1:c.196-29C=	ENSP00000414775.1:n.196-29C=
ENST00000432982.5:c.182-29C=
ENST00000444495.1:c.196-29C=	ENSP00000409142.1:n.196-29C=
ENST00000471832.1:n.127-29C=
ENST00000481054.5:n.197-29C=
ENST00000491144.5:n.544-29C=
ENST00000498831.1:n.52-29C=
NM_003907.2:c.196-29C=	NP_003898.2:n.196-29C=
XR_924208.1:n.1147-29C=
NM_003907.3:c.196-29C= MANE Select	NP_003898.2:n.196-29C=
XM_011513266.3:c.-706-29C=	XP_011511568.1:n.-706-29C=
XR_001740352.2:n.559-29C=
XR_001740353.2:n.559-29C=
XR_924208.2:n.559-29C=