Canonical Allele Identifier: CA2338166385

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905821G= , CM000681.2:g.44905821G=	GRCh38
NC_000019.9:g.45409078G= , CM000681.1:g.45409078G=	GRCh37
NC_000019.8:g.50100918G=	NCBI36
NG_007084.2:g.5040G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-44G= MANE Select	ENSP00000252486.3:n.-44G=
ENST00000252486.8:c.-44G=	ENSP00000252486.3:n.-44G=
ENST00000434152.5:c.-48G=	ENSP00000413653.2:n.-48G=
ENST00000446996.5:c.-59G=	ENSP00000413135.1:n.-59G=
ENST00000485628.2:n.26G=
NM_000041.3:c.-44G=	NP_000032.1:n.-44G=
NM_001302688.1:c.-48G=	NP_001289617.1:n.-48G=
NM_001302691.1:c.-59G=	NP_001289620.1:n.-59G=
NM_000041.4:c.-44G= MANE Select	NP_000032.1:n.-44G=
NM_001302688.2:c.-48G=	NP_001289617.1:n.-48G=
NM_001302691.2:c.-59G=	NP_001289620.1:n.-59G=