Canonical Allele Identifier: CA2338166388

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905824G= , CM000681.2:g.44905824G=	GRCh38
NC_000019.9:g.45409081G= , CM000681.1:g.45409081G=	GRCh37
NC_000019.8:g.50100921G=	NCBI36
NG_007084.2:g.5043G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-41G= MANE Select	ENSP00000252486.3:n.-41G=
ENST00000252486.8:c.-41G=	ENSP00000252486.3:n.-41G=
ENST00000434152.5:c.-45G=	ENSP00000413653.2:n.-45G=
ENST00000446996.5:c.-56G=	ENSP00000413135.1:n.-56G=
ENST00000485628.2:n.29G=
NM_000041.3:c.-41G=	NP_000032.1:n.-41G=
NM_001302688.1:c.-45G=	NP_001289617.1:n.-45G=
NM_001302691.1:c.-56G=	NP_001289620.1:n.-56G=
NM_000041.4:c.-41G= MANE Select	NP_000032.1:n.-41G=
NM_001302688.2:c.-45G=	NP_001289617.1:n.-45G=
NM_001302691.2:c.-56G=	NP_001289620.1:n.-56G=