Canonical Allele Identifier: CA2338167591

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908710C= , CM000681.2:g.44908710C=	GRCh38
NC_000019.9:g.45411967C= , CM000681.1:g.45411967C=	GRCh37
NC_000019.8:g.50103807C=	NCBI36
NG_007084.2:g.7929C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.414C= MANE Select	ENSP00000252486.3:p.Gly138=
ENST00000252486.8:c.414C=	ENSP00000252486.3:p.Gly138=
ENST00000425718.1:c.414C=	ENSP00000410423.1:p.Gly138=
ENST00000434152.5:c.492C=	ENSP00000413653.2:p.Gly164=
ENST00000446996.5:c.414C=	ENSP00000413135.1:p.Gly138=
NM_000041.3:c.414C=	NP_000032.1:p.Gly138=
NM_001302688.1:c.492C=	NP_001289617.1:p.Gly164=
NM_001302689.1:c.414C=	NP_001289618.1:p.Gly138=
NM_001302690.1:c.414C=	NP_001289619.1:p.Gly138=
NM_001302691.1:c.414C=	NP_001289620.1:p.Gly138=
NM_000041.4:c.414C= MANE Select	NP_000032.1:p.Gly138=
NM_001302688.2:c.492C=	NP_001289617.1:p.Gly164=
NM_001302689.2:c.414C=	NP_001289618.1:p.Gly138=
NM_001302691.2:c.414C=	NP_001289620.1:p.Gly138=
NM_001302690.2:c.414C=	NP_001289619.1:p.Gly138=