Canonical Allele Identifier: CA2338168139

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909226C= , CM000681.2:g.44909226C=	GRCh38
NC_000019.9:g.45412483C= , CM000681.1:g.45412483C=	GRCh37
NC_000019.8:g.50104323C=	NCBI36
NG_007084.2:g.8445C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.930C= MANE Select	ENSP00000252486.3:p.Ala310=
ENST00000252486.8:c.930C=	ENSP00000252486.3:p.Ala310=
NM_000041.3:c.930C=	NP_000032.1:p.Ala310=
NM_001302688.1:c.1008C=	NP_001289617.1:p.Ala336=
NM_001302689.1:c.930C=	NP_001289618.1:p.Ala310=
NM_001302690.1:c.930C=	NP_001289619.1:p.Ala310=
NM_001302691.1:c.930C=	NP_001289620.1:p.Ala310=
NM_000041.4:c.930C= MANE Select	NP_000032.1:p.Ala310=
NM_001302688.2:c.1008C=	NP_001289617.1:p.Ala336=
NM_001302689.2:c.930C=	NP_001289618.1:p.Ala310=
NM_001302691.2:c.930C=	NP_001289620.1:p.Ala310=
NM_001302690.2:c.930C=	NP_001289619.1:p.Ala310=