Canonical Allele Identifier: CA2695228865

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44908802_44908804dup , CM000681.2:g.44908802_44908804dup	GRCh38
NC_000019.9:g.45412059_45412061dup , CM000681.1:g.45412059_45412061dup	GRCh37
NC_000019.8:g.50103899_50103901dup	NCBI36
NG_007084.2:g.8021_8023dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.506_508dup MANE Select	ENSP00000252486.3:p.Asp169_Ala170insAsp
ENST00000252486.8:c.506_508dup	ENSP00000252486.3:p.Asp169_Ala170insAsp
ENST00000425718.1:c.506_508dup	ENSP00000410423.1:p.Asp169_Ala170insAsp
ENST00000434152.5:c.584_586dup	ENSP00000413653.2:p.Asp195_Ala196insAsp
ENST00000446996.5:c.506_508dup	ENSP00000413135.1:p.Asp169_Ala170insAsp
NM_000041.3:c.506_508dup	NP_000032.1:p.Asp169_Ala170insAsp
NM_001302688.1:c.584_586dup	NP_001289617.1:p.Asp195_Ala196insAsp
NM_001302689.1:c.506_508dup	NP_001289618.1:p.Asp169_Ala170insAsp
NM_001302690.1:c.506_508dup	NP_001289619.1:p.Asp169_Ala170insAsp
NM_001302691.1:c.506_508dup	NP_001289620.1:p.Asp169_Ala170insAsp
NM_000041.4:c.506_508dup MANE Select	NP_000032.1:p.Asp169_Ala170insAsp
NM_001302688.2:c.584_586dup	NP_001289617.1:p.Asp195_Ala196insAsp
NM_001302689.2:c.506_508dup	NP_001289618.1:p.Asp169_Ala170insAsp
NM_001302691.2:c.506_508dup	NP_001289620.1:p.Asp169_Ala170insAsp
NM_001302690.2:c.506_508dup	NP_001289619.1:p.Asp169_Ala170insAsp