Canonical Allele Identifier: CA2338167942

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908883G= , CM000681.2:g.44908883G=	GRCh38
NC_000019.9:g.45412140G= , CM000681.1:g.45412140G=	GRCh37
NC_000019.8:g.50103980G=	NCBI36
NG_007084.2:g.8102G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.587G= MANE Select	ENSP00000252486.3:p.Arg196=
ENST00000252486.8:c.587G=	ENSP00000252486.3:p.Arg196=
ENST00000425718.1:c.587G=	ENSP00000410423.1:p.Arg196=
ENST00000434152.5:c.665G=	ENSP00000413653.2:p.Arg222=
ENST00000446996.5:c.587G=	ENSP00000413135.1:p.Arg196=
NM_000041.3:c.587G=	NP_000032.1:p.Arg196=
NM_001302688.1:c.665G=	NP_001289617.1:p.Arg222=
NM_001302689.1:c.587G=	NP_001289618.1:p.Arg196=
NM_001302690.1:c.587G=	NP_001289619.1:p.Arg196=
NM_001302691.1:c.587G=	NP_001289620.1:p.Arg196=
NM_000041.4:c.587G= MANE Select	NP_000032.1:p.Arg196=
NM_001302688.2:c.665G=	NP_001289617.1:p.Arg222=
NM_001302689.2:c.587G=	NP_001289618.1:p.Arg196=
NM_001302691.2:c.587G=	NP_001289620.1:p.Arg196=
NM_001302690.2:c.587G=	NP_001289619.1:p.Arg196=