Canonical Allele Identifier: CA2338166382

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905816T= , CM000681.2:g.44905816T=	GRCh38
NC_000019.9:g.45409073T= , CM000681.1:g.45409073T=	GRCh37
NC_000019.8:g.50100913T=	NCBI36
NG_007084.2:g.5035T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-49T= MANE Select	ENSP00000252486.3:n.-49T=
ENST00000252486.8:c.-49T=	ENSP00000252486.3:n.-49T=
ENST00000434152.5:c.-53T=	ENSP00000413653.2:n.-53T=
ENST00000446996.5:c.-64T=	ENSP00000413135.1:n.-64T=
ENST00000485628.2:n.21T=
NM_000041.3:c.-49T=	NP_000032.1:n.-49T=
NM_001302688.1:c.-53T=	NP_001289617.1:n.-53T=
NM_001302691.1:c.-64T=	NP_001289620.1:n.-64T=
NM_000041.4:c.-49T= MANE Select	NP_000032.1:n.-49T=
NM_001302688.2:c.-53T=	NP_001289617.1:n.-53T=
NM_001302691.2:c.-64T=	NP_001289620.1:n.-64T=