Canonical Allele Identifier: CA2338166379

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905813A= , CM000681.2:g.44905813A=	GRCh38
NC_000019.9:g.45409070A= , CM000681.1:g.45409070A=	GRCh37
NC_000019.8:g.50100910A=	NCBI36
NG_007084.2:g.5032A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.-52A= MANE Select	ENSP00000252486.3:n.-52A=
ENST00000252486.8:c.-52A=	ENSP00000252486.3:n.-52A=
ENST00000434152.5:c.-56A=	ENSP00000413653.2:n.-56A=
ENST00000446996.5:c.-67A=	ENSP00000413135.1:n.-67A=
ENST00000485628.2:n.18A=
NM_000041.3:c.-52A=	NP_000032.1:n.-52A=
NM_001302688.1:c.-56A=	NP_001289617.1:n.-56A=
NM_001302691.1:c.-67A=	NP_001289620.1:n.-67A=
NM_000041.4:c.-52A= MANE Select	NP_000032.1:n.-52A=
NM_001302688.2:c.-56A=	NP_001289617.1:n.-56A=
NM_001302691.2:c.-67A=	NP_001289620.1:n.-67A=