Canonical Allele Identifier: CA2338167987
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44908975_44908976delinsGC , CM000681.2:g.44908975_44908976delinsGC GRCh38
NC_000019.9:g.45412232_45412233delinsGC , CM000681.1:g.45412232_45412233delinsGC GRCh37
NC_000019.8:g.50104072_50104073delinsGC NCBI36
NG_007084.2:g.8194_8195delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000252486.9:c.679_680delinsGC MANE Select ENSP00000252486.3:p.Ala227=
ENST00000252486.8:c.679_680delinsGC ENSP00000252486.3:p.Ala227=
ENST00000434152.5:c.757_758delinsGC ENSP00000413653.2:p.Ala253=
NM_000041.3:c.679_680delinsGC NP_000032.1:p.Ala227=
NM_001302688.1:c.757_758delinsGC NP_001289617.1:p.Ala253=
NM_001302689.1:c.679_680delinsGC NP_001289618.1:p.Ala227=
NM_001302690.1:c.679_680delinsGC NP_001289619.1:p.Ala227=
NM_001302691.1:c.679_680delinsGC NP_001289620.1:p.Ala227=
NM_000041.4:c.679_680delinsGC MANE Select NP_000032.1:p.Ala227=
NM_001302688.2:c.757_758delinsGC NP_001289617.1:p.Ala253=
NM_001302689.2:c.679_680delinsGC NP_001289618.1:p.Ala227=
NM_001302691.2:c.679_680delinsGC NP_001289620.1:p.Ala227=
NM_001302690.2:c.679_680delinsGC NP_001289619.1:p.Ala227=