Canonical Allele Identifier: CA2338166460

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905942C= , CM000681.2:g.44905942C=	GRCh38
NC_000019.9:g.45409199C= , CM000681.1:g.45409199C=	GRCh37
NC_000019.8:g.50101039C=	NCBI36
NG_007084.2:g.5161C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.-24+101C= MANE Select	ENSP00000252486.3:n.-24+101C=
ENST00000252486.8:c.-24+101C=	ENSP00000252486.3:n.-24+101C=
ENST00000434152.5:c.55+19C=	ENSP00000413653.2:n.55+19C=
ENST00000446996.5:c.-39+101C=	ENSP00000413135.1:n.-39+101C=
ENST00000485628.2:n.46+101C=
NM_000041.3:c.-24+101C=	NP_000032.1:n.-24+101C=
NM_001302688.1:c.55+19C=	NP_001289617.1:n.55+19C=
NM_001302691.1:c.-39+101C=	NP_001289620.1:n.-39+101C=
NM_000041.4:c.-24+101C= MANE Select	NP_000032.1:n.-24+101C=
NM_001302688.2:c.55+19C=	NP_001289617.1:n.55+19C=
NM_001302691.2:c.-39+101C=	NP_001289620.1:n.-39+101C=