Canonical Allele Identifier: CA2585715133

Gene: APOE

Linked Data

• gnomAD v4: 19-44907632-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907638dup , CM000681.2:g.44907638dup	GRCh38
NC_000019.9:g.45410895dup , CM000681.1:g.45410895dup	GRCh37
NC_000019.8:g.50102735dup	NCBI36
NG_007084.2:g.6857dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.44-122dup MANE Select	ENSP00000252486.3:n.44-122dup
ENST00000252486.8:c.44-122dup	ENSP00000252486.3:n.44-122dup
ENST00000425718.1:c.44-122dup	ENSP00000410423.1:n.44-122dup
ENST00000434152.5:c.122-122dup	ENSP00000413653.2:n.122-122dup
ENST00000446996.5:c.44-122dup	ENSP00000413135.1:n.44-122dup
NM_000041.3:c.44-122dup	NP_000032.1:n.44-122dup
NM_001302688.1:c.122-122dup	NP_001289617.1:n.122-122dup
NM_001302689.1:c.44-122dup	NP_001289618.1:n.44-122dup
NM_001302690.1:c.44-122dup	NP_001289619.1:n.44-122dup
NM_001302691.1:c.44-122dup	NP_001289620.1:n.44-122dup
NM_000041.4:c.44-122dup MANE Select	NP_000032.1:n.44-122dup
NM_001302688.2:c.122-122dup	NP_001289617.1:n.122-122dup
NM_001302689.2:c.44-122dup	NP_001289618.1:n.44-122dup
NM_001302691.2:c.44-122dup	NP_001289620.1:n.44-122dup
NM_001302690.2:c.44-122dup	NP_001289619.1:n.44-122dup