Canonical Allele Identifier: CA2616111331

Gene: APOC3

Linked Data

• gnomAD v4: 11-116832969-CTTAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832970_116832974del , CM000673.2:g.116832970_116832974del	GRCh38
NC_000011.9:g.116703686_116703690del , CM000673.1:g.116703686_116703690del	GRCh37
NC_000011.8:g.116208896_116208900del	NCBI36
NG_008949.1:g.8063_8067del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000227667.8:c.*86_*90del MANE Select	ENSP00000227667.2:n.*86_*90del
ENST00000227667.7:c.*86_*90del	ENSP00000227667.2:n.*86_*90del
ENST00000375345.3:c.*86_*90del	ENSP00000364494.1:n.*86_*90del
ENST00000630701.1:c.440_444del	ENSP00000486182.1:n.440_444del
NM_000040.1:c.*86_*90del	NP_000031.1:n.*86_*90del
NM_000040.2:c.*86_*90del	NP_000031.1:n.*86_*90del
NM_000040.3:c.*86_*90del MANE Select	NP_000031.1:n.*86_*90del