Canonical Allele Identifier: CA2338166390

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905829T= , CM000681.2:g.44905829T=	GRCh38
NC_000019.9:g.45409086T= , CM000681.1:g.45409086T=	GRCh37
NC_000019.8:g.50100926T=	NCBI36
NG_007084.2:g.5048T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-36T= MANE Select	ENSP00000252486.3:n.-36T=
ENST00000252486.8:c.-36T=	ENSP00000252486.3:n.-36T=
ENST00000434152.5:c.-40T=	ENSP00000413653.2:n.-40T=
ENST00000446996.5:c.-51T=	ENSP00000413135.1:n.-51T=
ENST00000485628.2:n.34T=
NM_000041.3:c.-36T=	NP_000032.1:n.-36T=
NM_001302688.1:c.-40T=	NP_001289617.1:n.-40T=
NM_001302691.1:c.-51T=	NP_001289620.1:n.-51T=
NM_000041.4:c.-36T= MANE Select	NP_000032.1:n.-36T=
NM_001302688.2:c.-40T=	NP_001289617.1:n.-40T=
NM_001302691.2:c.-51T=	NP_001289620.1:n.-51T=