Canonical Allele Identifier: CA2338166386

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905823C= , CM000681.2:g.44905823C=	GRCh38
NC_000019.9:g.45409080C= , CM000681.1:g.45409080C=	GRCh37
NC_000019.8:g.50100920C=	NCBI36
NG_007084.2:g.5042C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.-42C= MANE Select	ENSP00000252486.3:n.-42C=
ENST00000252486.8:c.-42C=	ENSP00000252486.3:n.-42C=
ENST00000434152.5:c.-46C=	ENSP00000413653.2:n.-46C=
ENST00000446996.5:c.-57C=	ENSP00000413135.1:n.-57C=
ENST00000485628.2:n.28C=
NM_000041.3:c.-42C=	NP_000032.1:n.-42C=
NM_001302688.1:c.-46C=	NP_001289617.1:n.-46C=
NM_001302691.1:c.-57C=	NP_001289620.1:n.-57C=
NM_000041.4:c.-42C= MANE Select	NP_000032.1:n.-42C=
NM_001302688.2:c.-46C=	NP_001289617.1:n.-46C=
NM_001302691.2:c.-57C=	NP_001289620.1:n.-57C=