Canonical Allele Identifier: CA2002760368

Gene: APOC3

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.116832973_116832976delinsAAAG , CM000673.2:g.116832973_116832976delinsAAAG	GRCh38
NC_000011.9:g.116703689_116703692delinsAAAG , CM000673.1:g.116703689_116703692delinsAAAG	GRCh37
NC_000011.8:g.116208899_116208902delinsAAAG	NCBI36
NG_008949.1:g.8066_8069delinsAAAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000227667.8:c.*89_*92delinsAAAG MANE Select	ENSP00000227667.2:n.*89_*92delinsAAAG
ENST00000227667.7:c.*89_*92delinsAAAG	ENSP00000227667.2:n.*89_*92delinsAAAG
ENST00000375345.3:c.*89_*92delinsAAAG	ENSP00000364494.1:n.*89_*92delinsAAAG
ENST00000630701.1:c.443_446delinsAAAG	ENSP00000486182.1:n.443_446delinsAAAG
NM_000040.1:c.*89_*92delinsAAAG	NP_000031.1:n.*89_*92delinsAAAG
NM_000040.2:c.*89_*92delinsAAAG	NP_000031.1:n.*89_*92delinsAAAG
NM_000040.3:c.*89_*92delinsAAAG MANE Select	NP_000031.1:n.*89_*92delinsAAAG