Canonical Allele Identifier: CA2574986549

Gene: APOC3

Linked Data

• gnomAD v4: 11-116830616-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116830617dup , CM000673.2:g.116830617dup	GRCh38
NC_000011.9:g.116701333dup , CM000673.1:g.116701333dup	GRCh37
NC_000011.8:g.116206543dup	NCBI36
NG_008949.1:g.5710dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.35dup MANE Select	ENSP00000227667.2:p.Ala13GlyfsTer?
ENST00000227667.7:c.35dup	ENSP00000227667.2:p.Ala13GlyfsTer?
ENST00000375345.3:c.89dup	ENSP00000364494.1:p.Ala31GlyfsTer?
ENST00000433777.5:c.35dup	ENSP00000410614.1:p.Ala13GlyfsTer?
ENST00000470144.1:n.67dup
ENST00000630701.1:c.89dup	ENSP00000486182.1:p.Ala31GlyfsTer?
NM_000040.1:c.35dup	NP_000031.1:p.Ala13GlyfsTer?
NM_000040.2:c.35dup	NP_000031.1:p.Ala13GlyfsTer?
NM_000040.3:c.35dup MANE Select	NP_000031.1:p.Ala13GlyfsTer?