Canonical Allele Identifier: CA654624848
Gene: APOC3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116830539_116830540insAA , CM000673.2:g.116830539_116830540insAA GRCh38
NC_000011.9:g.116701255_116701256insAA , CM000673.1:g.116701255_116701256insAA GRCh37
NC_000011.8:g.116206465_116206466insAA NCBI36
NG_008949.1:g.5632_5633insAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000227667.8:c.-13-31_-13-30insAA MANE Select ENSP00000227667.2:n.-13-31_-13-30insAA
ENST00000227667.7:c.-13-31_-13-30insAA ENSP00000227667.2:n.-13-31_-13-30insAA
ENST00000375345.3:c.11_12insAA ENSP00000364494.1:p.Trp4Ter
ENST00000433777.5:c.-13-31_-13-30insAA ENSP00000410614.1:n.-13-31_-13-30insAA
ENST00000470144.1:n.20-31_20-30insAA
ENST00000630701.1:c.11_12insAA ENSP00000486182.1:p.Trp4Ter
NM_000040.1:c.-13-31_-13-30insAA NP_000031.1:n.-13-31_-13-30insAA
NM_000040.2:c.-13-31_-13-30insAA NP_000031.1:n.-13-31_-13-30insAA
NM_000040.3:c.-13-31_-13-30insAA MANE Select NP_000031.1:n.-13-31_-13-30insAA