Canonical Allele Identifier: CA2585713762
Gene: APOE HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.44905815del , CM000681.2:g.44905815del GRCh38
NC_000019.9:g.45409072del , CM000681.1:g.45409072del GRCh37
NC_000019.8:g.50100912del NCBI36
NG_007084.2:g.5034del

Transcript Alleles

HGVS Amino-acid Change
ENST00000252486.9:c.-50del MANE Select ENSP00000252486.3:n.-50del
ENST00000252486.8:c.-50del ENSP00000252486.3:n.-50del
ENST00000434152.5:c.-54del ENSP00000413653.2:n.-54del
ENST00000446996.5:c.-65del ENSP00000413135.1:n.-65del
ENST00000485628.2:n.20del
NM_000041.3:c.-50del NP_000032.1:n.-50del
NM_001302688.1:c.-54del NP_001289617.1:n.-54del
NM_001302691.1:c.-65del NP_001289620.1:n.-65del
NM_000041.4:c.-50del MANE Select NP_000032.1:n.-50del
NM_001302688.2:c.-54del NP_001289617.1:n.-54del
NM_001302691.2:c.-65del NP_001289620.1:n.-65del