Canonical Allele Identifier: CA340483885

Gene: PCSK9

Linked Data

• dbSNP Id: rs377361152
• MyVariant Identifiers: chr1:g.55509705C>A (hg19) ; chr1:g.55044032C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55044032C>A , CM000663.2:g.55044032C>A	GRCh38
NC_000001.10:g.55509705C>A , CM000663.1:g.55509705C>A	GRCh37
NC_000001.9:g.55282293C>A	NCBI36
NG_009061.1:g.9486C>A , LRG_275:g.9486C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.397C>A	ENSP00000501161.2:p.Leu133Met
ENST00000710286.1:c.754C>A	ENSP00000518176.1:p.Leu252Met
ENST00000673662.1:n.67C>A
ENST00000673726.1:c.397C>A	ENSP00000501004.1:p.Leu133Met
ENST00000673903.1:c.22C>A	ENSP00000501257.1:p.Leu8Met
ENST00000302118.5:c.397C>A MANE Select	ENSP00000303208.5:p.Leu133Met
NM_174936.3:c.397C>A , LRG_275t1:c.397C>A	NP_777596.2:p.Leu133Met
NR_110451.1:n.182+3629C>A
NM_174936.4:c.397C>A MANE Select	NP_777596.2:p.Leu133Met
NR_110451.2:n.182+3629C>A