Canonical Allele Identifier: CA2585715223

Gene: APOE

Linked Data

• gnomAD v4: 19-44907853-TG-T

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.139del MANE Select	ENSP00000252486.3:p.Ala47HisfsTer?
ENST00000252486.8:c.139del	ENSP00000252486.3:p.Ala47HisfsTer?
ENST00000425718.1:c.139del	ENSP00000410423.1:p.Ala47HisfsTer?
ENST00000434152.5:c.217del	ENSP00000413653.2:p.Ala73HisfsTer?
ENST00000446996.5:c.139del	ENSP00000413135.1:p.Ala47HisfsTer?
NM_000041.3:c.139del	NP_000032.1:p.Ala47HisfsTer?
NM_001302688.1:c.217del	NP_001289617.1:p.Ala73HisfsTer?
NM_001302689.1:c.139del	NP_001289618.1:p.Ala47HisfsTer?
NM_001302690.1:c.139del	NP_001289619.1:p.Ala47HisfsTer?
NM_001302691.1:c.139del	NP_001289620.1:p.Ala47HisfsTer?
NM_000041.4:c.139del MANE Select	NP_000032.1:p.Ala47HisfsTer?
NM_001302688.2:c.217del	NP_001289617.1:p.Ala73HisfsTer?
NM_001302689.2:c.139del	NP_001289618.1:p.Ala47HisfsTer?
NM_001302691.2:c.139del	NP_001289620.1:p.Ala47HisfsTer?
NM_001302690.2:c.139del	NP_001289619.1:p.Ala47HisfsTer?