Canonical Allele Identifier: CA2338167489

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908662G= , CM000681.2:g.44908662G=	GRCh38
NC_000019.9:g.45411919G= , CM000681.1:g.45411919G=	GRCh37
NC_000019.8:g.50103759G=	NCBI36
NG_007084.2:g.7881G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.366G= MANE Select	ENSP00000252486.3:p.Leu122=
ENST00000252486.8:c.366G=	ENSP00000252486.3:p.Leu122=
ENST00000425718.1:c.366G=	ENSP00000410423.1:p.Leu122=
ENST00000434152.5:c.444G=	ENSP00000413653.2:p.Leu148=
ENST00000446996.5:c.366G=	ENSP00000413135.1:p.Leu122=
NM_000041.3:c.366G=	NP_000032.1:p.Leu122=
NM_001302688.1:c.444G=	NP_001289617.1:p.Leu148=
NM_001302689.1:c.366G=	NP_001289618.1:p.Leu122=
NM_001302690.1:c.366G=	NP_001289619.1:p.Leu122=
NM_001302691.1:c.366G=	NP_001289620.1:p.Leu122=
NM_000041.4:c.366G= MANE Select	NP_000032.1:p.Leu122=
NM_001302688.2:c.444G=	NP_001289617.1:p.Leu148=
NM_001302689.2:c.366G=	NP_001289618.1:p.Leu122=
NM_001302691.2:c.366G=	NP_001289620.1:p.Leu122=
NM_001302690.2:c.366G=	NP_001289619.1:p.Leu122=