Canonical Allele Identifier: CA1140578550
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55039880_55039902delinsCTGCTGCTGCTGCTGCTGCTGCT , CM000663.2:g.55039880_55039902delinsCTGCTGCTGCTGCTGCTGCTGCT GRCh38
NC_000001.10:g.55505553_55505575delinsCTGCTGCTGCTGCTGCTGCTGCT , CM000663.1:g.55505553_55505575delinsCTGCTGCTGCTGCTGCTGCTGCT GRCh37
NC_000001.9:g.55278141_55278163delinsCTGCTGCTGCTGCTGCTGCTGCT NCBI36
NG_009061.1:g.5334_5356delinsCTGCTGCTGCTGCTGCTGCTGCT , LRG_275:g.5334_5356delinsCTGCTGCTGCTGCTGCTGCTGCT

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.43_65delinsCTGCTGCTGCTGCTGCTGCTGCT ENSP00000501161.2:p.Leu15=
ENST00000710286.1:c.400_422delinsCTGCTGCTGCTGCTGCTGCTGCT ENSP00000518176.1:p.Leu134=
ENST00000673726.1:c.43_65delinsCTGCTGCTGCTGCTGCTGCTGCT ENSP00000501004.1:p.Leu15=
ENST00000302118.5:c.43_65delinsCTGCTGCTGCTGCTGCTGCTGCT MANE Select ENSP00000303208.5:p.Leu15=
NM_174936.3:c.43_65delinsCTGCTGCTGCTGCTGCTGCTGCT , LRG_275t1:c.43_65delinsCTGCTGCTGCTGCTGCTGCTGCT NP_777596.2:p.Leu15=
NM_174936.4:c.43_65delinsCTGCTGCTGCTGCTGCTGCTGCT MANE Select NP_777596.2:p.Leu15=