Canonical Allele Identifier: CA2338167866

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908772T= , CM000681.2:g.44908772T=	GRCh38
NC_000019.9:g.45412029T= , CM000681.1:g.45412029T=	GRCh37
NC_000019.8:g.50103869T=	NCBI36
NG_007084.2:g.7991T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.476T= MANE Select	ENSP00000252486.3:p.Leu159=
ENST00000252486.8:c.476T=	ENSP00000252486.3:p.Leu159=
ENST00000425718.1:c.476T=	ENSP00000410423.1:p.Leu159=
ENST00000434152.5:c.554T=	ENSP00000413653.2:p.Leu185=
ENST00000446996.5:c.476T=	ENSP00000413135.1:p.Leu159=
NM_000041.3:c.476T=	NP_000032.1:p.Leu159=
NM_001302688.1:c.554T=	NP_001289617.1:p.Leu185=
NM_001302689.1:c.476T=	NP_001289618.1:p.Leu159=
NM_001302690.1:c.476T=	NP_001289619.1:p.Leu159=
NM_001302691.1:c.476T=	NP_001289620.1:p.Leu159=
NM_000041.4:c.476T= MANE Select	NP_000032.1:p.Leu159=
NM_001302688.2:c.554T=	NP_001289617.1:p.Leu185=
NM_001302689.2:c.476T=	NP_001289618.1:p.Leu159=
NM_001302691.2:c.476T=	NP_001289620.1:p.Leu159=
NM_001302690.2:c.476T=	NP_001289619.1:p.Leu159=