Canonical Allele Identifier: CA2338168007

Gene: APOE

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.44909003_44909006delinsTGGA , CM000681.2:g.44909003_44909006delinsTGGA	GRCh38
NC_000019.9:g.45412260_45412263delinsTGGA , CM000681.1:g.45412260_45412263delinsTGGA	GRCh37
NC_000019.8:g.50104100_50104103delinsTGGA	NCBI36
NG_007084.2:g.8222_8225delinsTGGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000252486.9:c.707_710delinsTGGA MANE Select	ENSP00000252486.3:p.Met236=
ENST00000252486.8:c.707_710delinsTGGA	ENSP00000252486.3:p.Met236=
ENST00000434152.5:c.785_788delinsTGGA	ENSP00000413653.2:p.Met262=
NM_000041.3:c.707_710delinsTGGA	NP_000032.1:p.Met236=
NM_001302688.1:c.785_788delinsTGGA	NP_001289617.1:p.Met262=
NM_001302689.1:c.707_710delinsTGGA	NP_001289618.1:p.Met236=
NM_001302690.1:c.707_710delinsTGGA	NP_001289619.1:p.Met236=
NM_001302691.1:c.707_710delinsTGGA	NP_001289620.1:p.Met236=
NM_000041.4:c.707_710delinsTGGA MANE Select	NP_000032.1:p.Met236=
NM_001302688.2:c.785_788delinsTGGA	NP_001289617.1:p.Met262=
NM_001302689.2:c.707_710delinsTGGA	NP_001289618.1:p.Met236=
NM_001302691.2:c.707_710delinsTGGA	NP_001289620.1:p.Met236=
NM_001302690.2:c.707_710delinsTGGA	NP_001289619.1:p.Met236=