Canonical Allele Identifier: CA2585713772

Gene: APOE

Linked Data

• gnomAD v4: 19-44905825-T-TC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44905827dup , CM000681.2:g.44905827dup	GRCh38
NC_000019.9:g.45409084dup , CM000681.1:g.45409084dup	GRCh37
NC_000019.8:g.50100924dup	NCBI36
NG_007084.2:g.5046dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.-38dup MANE Select	ENSP00000252486.3:n.-38dup
ENST00000252486.8:c.-38dup	ENSP00000252486.3:n.-38dup
ENST00000434152.5:c.-42dup	ENSP00000413653.2:n.-42dup
ENST00000446996.5:c.-53dup	ENSP00000413135.1:n.-53dup
ENST00000485628.2:n.32dup
NM_000041.3:c.-38dup	NP_000032.1:n.-38dup
NM_001302688.1:c.-42dup	NP_001289617.1:n.-42dup
NM_001302691.1:c.-53dup	NP_001289620.1:n.-53dup
NM_000041.4:c.-38dup MANE Select	NP_000032.1:n.-38dup
NM_001302688.2:c.-42dup	NP_001289617.1:n.-42dup
NM_001302691.2:c.-53dup	NP_001289620.1:n.-53dup