Canonical Allele Identifier: CA2338167613

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908714G= , CM000681.2:g.44908714G=	GRCh38
NC_000019.9:g.45411971G= , CM000681.1:g.45411971G=	GRCh37
NC_000019.8:g.50103811G=	NCBI36
NG_007084.2:g.7933G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.418G= MANE Select	ENSP00000252486.3:p.Val140=
ENST00000252486.8:c.418G=	ENSP00000252486.3:p.Val140=
ENST00000425718.1:c.418G=	ENSP00000410423.1:p.Val140=
ENST00000434152.5:c.496G=	ENSP00000413653.2:p.Val166=
ENST00000446996.5:c.418G=	ENSP00000413135.1:p.Val140=
NM_000041.3:c.418G=	NP_000032.1:p.Val140=
NM_001302688.1:c.496G=	NP_001289617.1:p.Val166=
NM_001302689.1:c.418G=	NP_001289618.1:p.Val140=
NM_001302690.1:c.418G=	NP_001289619.1:p.Val140=
NM_001302691.1:c.418G=	NP_001289620.1:p.Val140=
NM_000041.4:c.418G= MANE Select	NP_000032.1:p.Val140=
NM_001302688.2:c.496G=	NP_001289617.1:p.Val166=
NM_001302689.2:c.418G=	NP_001289618.1:p.Val140=
NM_001302691.2:c.418G=	NP_001289620.1:p.Val140=
NM_001302690.2:c.418G=	NP_001289619.1:p.Val140=