Canonical Allele Identifier: CA2338167291

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44907695_44907696delinsCT , CM000681.2:g.44907695_44907696delinsCT	GRCh38
NC_000019.9:g.45410952_45410953delinsCT , CM000681.1:g.45410952_45410953delinsCT	GRCh37
NC_000019.8:g.50102792_50102793delinsCT	NCBI36
NG_007084.2:g.6914_6915delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252486.9:c.44-65_44-64delinsCT MANE Select	ENSP00000252486.3:n.44-65_44-64delinsCT
ENST00000252486.8:c.44-65_44-64delinsCT	ENSP00000252486.3:n.44-65_44-64delinsCT
ENST00000425718.1:c.44-65_44-64delinsCT	ENSP00000410423.1:n.44-65_44-64delinsCT
ENST00000434152.5:c.122-65_122-64delinsCT	ENSP00000413653.2:n.122-65_122-64delinsCT
ENST00000446996.5:c.44-65_44-64delinsCT	ENSP00000413135.1:n.44-65_44-64delinsCT
NM_000041.3:c.44-65_44-64delinsCT	NP_000032.1:n.44-65_44-64delinsCT
NM_001302688.1:c.122-65_122-64delinsCT	NP_001289617.1:n.122-65_122-64delinsCT
NM_001302689.1:c.44-65_44-64delinsCT	NP_001289618.1:n.44-65_44-64delinsCT
NM_001302690.1:c.44-65_44-64delinsCT	NP_001289619.1:n.44-65_44-64delinsCT
NM_001302691.1:c.44-65_44-64delinsCT	NP_001289620.1:n.44-65_44-64delinsCT
NM_000041.4:c.44-65_44-64delinsCT MANE Select	NP_000032.1:n.44-65_44-64delinsCT
NM_001302688.2:c.122-65_122-64delinsCT	NP_001289617.1:n.122-65_122-64delinsCT
NM_001302689.2:c.44-65_44-64delinsCT	NP_001289618.1:n.44-65_44-64delinsCT
NM_001302691.2:c.44-65_44-64delinsCT	NP_001289620.1:n.44-65_44-64delinsCT
NM_001302690.2:c.44-65_44-64delinsCT	NP_001289619.1:n.44-65_44-64delinsCT