Canonical Allele Identifier: CA2616111319
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116832953_116832954del , CM000673.2:g.116832953_116832954del GRCh38
NC_000011.9:g.116703669_116703670del , CM000673.1:g.116703669_116703670del GRCh37
NC_000011.8:g.116208879_116208880del NCBI36
NG_008949.1:g.8046_8047del

Transcript Alleles

HGVS Amino-acid change
ENST00000227667.8:c.*69_*70del MANE Select ENSP00000227667.2:n.*69_*70del
ENST00000227667.7:c.*69_*70del ENSP00000227667.2:n.*69_*70del
ENST00000375345.3:c.*69_*70del ENSP00000364494.1:n.*69_*70del
ENST00000630701.1:c.423_424del ENSP00000486182.1:n.423_424del
NM_000040.1:c.*69_*70del NP_000031.1:n.*69_*70del
NM_000040.2:c.*69_*70del NP_000031.1:n.*69_*70del
NM_000040.3:c.*69_*70del MANE Select NP_000031.1:n.*69_*70del