Canonical Allele Identifier: CA2338168002

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908997C= , CM000681.2:g.44908997C=	GRCh38
NC_000019.9:g.45412254C= , CM000681.1:g.45412254C=	GRCh37
NC_000019.8:g.50104094C=	NCBI36
NG_007084.2:g.8216C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.701C= MANE Select	ENSP00000252486.3:p.Ala234=
ENST00000252486.8:c.701C=	ENSP00000252486.3:p.Ala234=
ENST00000434152.5:c.779C=	ENSP00000413653.2:p.Ala260=
NM_000041.3:c.701C=	NP_000032.1:p.Ala234=
NM_001302688.1:c.779C=	NP_001289617.1:p.Ala260=
NM_001302689.1:c.701C=	NP_001289618.1:p.Ala234=
NM_001302690.1:c.701C=	NP_001289619.1:p.Ala234=
NM_001302691.1:c.701C=	NP_001289620.1:p.Ala234=
NM_000041.4:c.701C= MANE Select	NP_000032.1:p.Ala234=
NM_001302688.2:c.779C=	NP_001289617.1:p.Ala260=
NM_001302689.2:c.701C=	NP_001289618.1:p.Ala234=
NM_001302691.2:c.701C=	NP_001289620.1:p.Ala234=
NM_001302690.2:c.701C=	NP_001289619.1:p.Ala234=