Canonical Allele Identifier: CA2840306790
Gene: APOE HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44909060_44909062del , CM000681.2:g.44909060_44909062del GRCh38
NC_000019.9:g.45412317_45412319del , CM000681.1:g.45412317_45412319del GRCh37
NC_000019.8:g.50104157_50104159del NCBI36
NG_007084.2:g.8279_8281del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.764_766del MANE Select ENSP00000252486.3:p.Ala255del
ENST00000252486.8:c.764_766del ENSP00000252486.3:p.Ala255del
NM_000041.3:c.764_766del NP_000032.1:p.Ala255del
NM_001302688.1:c.842_844del NP_001289617.1:p.Ala281del
NM_001302689.1:c.764_766del NP_001289618.1:p.Ala255del
NM_001302690.1:c.764_766del NP_001289619.1:p.Ala255del
NM_001302691.1:c.764_766del NP_001289620.1:p.Ala255del
NM_000041.4:c.764_766del MANE Select NP_000032.1:p.Ala255del
NM_001302688.2:c.842_844del NP_001289617.1:p.Ala281del
NM_001302689.2:c.764_766del NP_001289618.1:p.Ala255del
NM_001302691.2:c.764_766del NP_001289620.1:p.Ala255del
NM_001302690.2:c.764_766del NP_001289619.1:p.Ala255del