Canonical Allele Identifier: CA2338168026

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909025C= , CM000681.2:g.44909025C=	GRCh38
NC_000019.9:g.45412282C= , CM000681.1:g.45412282C=	GRCh37
NC_000019.8:g.50104122C=	NCBI36
NG_007084.2:g.8244C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.729C= MANE Select	ENSP00000252486.3:p.Thr243=
ENST00000252486.8:c.729C=	ENSP00000252486.3:p.Thr243=
ENST00000434152.5:c.807C=	ENSP00000413653.2:p.Thr269=
NM_000041.3:c.729C=	NP_000032.1:p.Thr243=
NM_001302688.1:c.807C=	NP_001289617.1:p.Thr269=
NM_001302689.1:c.729C=	NP_001289618.1:p.Thr243=
NM_001302690.1:c.729C=	NP_001289619.1:p.Thr243=
NM_001302691.1:c.729C=	NP_001289620.1:p.Thr243=
NM_000041.4:c.729C= MANE Select	NP_000032.1:p.Thr243=
NM_001302688.2:c.807C=	NP_001289617.1:p.Thr269=
NM_001302689.2:c.729C=	NP_001289618.1:p.Thr243=
NM_001302691.2:c.729C=	NP_001289620.1:p.Thr243=
NM_001302690.2:c.729C=	NP_001289619.1:p.Thr243=