Canonical Allele Identifier: CA2585715468

Gene: APOE

Linked Data

• gnomAD v4: 19-44909120-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909122del , CM000681.2:g.44909122del	GRCh38
NC_000019.9:g.45412379del , CM000681.1:g.45412379del	GRCh37
NC_000019.8:g.50104219del	NCBI36
NG_007084.2:g.8341del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.826del MANE Select	ENSP00000252486.3:p.Gln276ArgfsTer?
ENST00000252486.8:c.826del	ENSP00000252486.3:p.Gln276ArgfsTer?
NM_000041.3:c.826del	NP_000032.1:p.Gln276ArgfsTer?
NM_001302688.1:c.904del	NP_001289617.1:p.Gln302ArgfsTer?
NM_001302689.1:c.826del	NP_001289618.1:p.Gln276ArgfsTer?
NM_001302690.1:c.826del	NP_001289619.1:p.Gln276ArgfsTer?
NM_001302691.1:c.826del	NP_001289620.1:p.Gln276ArgfsTer?
NM_000041.4:c.826del MANE Select	NP_000032.1:p.Gln276ArgfsTer?
NM_001302688.2:c.904del	NP_001289617.1:p.Gln302ArgfsTer?
NM_001302689.2:c.826del	NP_001289618.1:p.Gln276ArgfsTer?
NM_001302691.2:c.826del	NP_001289620.1:p.Gln276ArgfsTer?
NM_001302690.2:c.826del	NP_001289619.1:p.Gln276ArgfsTer?