Canonical Allele Identifier: CA1425882915

Gene: EIF2B5

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.184137963G= , CM000665.2:g.184137963G=	GRCh38
NC_000003.11:g.183855751G= , CM000665.1:g.183855751G=	GRCh37
NC_000003.10:g.185338445G=	NCBI36
NG_015826.1:g.7942G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000465218.3:n.595G=
ENST00000468748.7:n.555G=
ENST00000484154.2:n.1193G=
ENST00000491008.6:n.1320G=
ENST00000492226.2:n.569G=
ENST00000492773.6:c.304G=
ENST00000647636.1:c.572G=	ENSP00000497505.1:p.Ser191=
ENST00000647909.1:c.596G=	ENSP00000498164.1:p.Ser199=
ENST00000648145.1:c.340G=
ENST00000648189.1:c.322G=
ENST00000648256.1:c.521G=	ENSP00000497356.1:p.Ser174=
ENST00000648314.1:c.572G=	ENSP00000496920.1:p.Ser191=
ENST00000648599.1:c.572G=	ENSP00000497159.1:p.Ser191=
ENST00000648630.1:c.566G=	ENSP00000497887.1:p.Ser189=
ENST00000648682.1:c.572G=	ENSP00000498185.1:p.Ser191=
ENST00000648882.1:c.*398G=	ENSP00000497603.1:n.*398G=
ENST00000648890.1:c.572G=	ENSP00000497503.1:p.Ser191=
ENST00000648915.2:c.572G= MANE Select	ENSP00000497160.1:p.Ser191=
ENST00000649545.1:c.306G=
ENST00000649688.1:c.572G=	ENSP00000497097.1:p.Ser191=
ENST00000649814.1:n.621G=
ENST00000650270.1:c.439G=
ENST00000273783.7:c.572G=	ENSP00000273783.3:p.Ser191=
ENST00000432982.5:c.245+1288G=
ENST00000444495.1:c.572G=	ENSP00000409142.1:p.Ser191=
ENST00000468748.5:n.25G=
ENST00000481054.5:n.573G=
ENST00000491008.5:n.536G=
ENST00000491144.5:n.1012G=
ENST00000498831.1:n.527G=
NM_003907.2:c.572G=	NP_003898.2:p.Ser191=
XR_924208.1:n.1523G=
NM_003907.3:c.572G= MANE Select	NP_003898.2:p.Ser191=
XM_011513266.3:c.-330G=	XP_011511568.1:n.-330G=
XR_001740352.2:n.935G=
XR_001740353.2:n.935G=
XR_924208.2:n.935G=