Canonical Allele Identifier: CA2960170683

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907855dup , CM000681.2:g.44907855dup	GRCh38
NC_000019.9:g.45411112dup , CM000681.1:g.45411112dup	GRCh37
NC_000019.8:g.50102952dup	NCBI36
NG_007084.2:g.7074dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.139dup MANE Select	ENSP00000252486.3:p.Ala47GlyfsTer17
ENST00000252486.8:c.139dup	ENSP00000252486.3:p.Ala47GlyfsTer17
ENST00000425718.1:c.139dup	ENSP00000410423.1:p.Ala47GlyfsTer17
ENST00000434152.5:c.217dup	ENSP00000413653.2:p.Ala73GlyfsTer17
ENST00000446996.5:c.139dup	ENSP00000413135.1:p.Ala47GlyfsTer17
NM_000041.3:c.139dup	NP_000032.1:p.Ala47GlyfsTer17
NM_001302688.1:c.217dup	NP_001289617.1:p.Ala73GlyfsTer17
NM_001302689.1:c.139dup	NP_001289618.1:p.Ala47GlyfsTer17
NM_001302690.1:c.139dup	NP_001289619.1:p.Ala47GlyfsTer17
NM_001302691.1:c.139dup	NP_001289620.1:p.Ala47GlyfsTer17
NM_000041.4:c.139dup MANE Select	NP_000032.1:p.Ala47GlyfsTer17
NM_001302688.2:c.217dup	NP_001289617.1:p.Ala73GlyfsTer17
NM_001302689.2:c.139dup	NP_001289618.1:p.Ala47GlyfsTer17
NM_001302691.2:c.139dup	NP_001289620.1:p.Ala47GlyfsTer17
NM_001302690.2:c.139dup	NP_001289619.1:p.Ala47GlyfsTer17