Canonical Allele Identifier: CA1167985013

Gene: PCSK9

Linked Data

• dbSNP Id: rs1644745944
• gnomAD v4: 1-55059789-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059790del , CM000663.2:g.55059790del	GRCh38
NC_000001.10:g.55525463del , CM000663.1:g.55525463del	GRCh37
NC_000001.9:g.55298051del	NCBI36
NG_009061.1:g.25244del , LRG_275:g.25244del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1681+127del	ENSP00000501161.2:n.1681+127del
ENST00000710286.1:c.2038+127del	ENSP00000518176.1:n.2038+127del
ENST00000673903.1:c.1306+127del	ENSP00000501257.1:n.1306+127del
ENST00000673913.1:c.421+127del	ENSP00000501161.1:n.421+127del
ENST00000302118.5:c.1681+127del MANE Select	ENSP00000303208.5:n.1681+127del
ENST00000490692.1:n.2227+1143del
NM_174936.3:c.1681+127del , LRG_275t1:c.1681+127del	NP_777596.2:n.1681+127del
NR_110451.1:n.1288+127del
XM_011541193.1:c.802+127del	XP_011539495.1:n.802+127del
NM_174936.4:c.1681+127del MANE Select	NP_777596.2:n.1681+127del
NR_110451.2:n.1288+127del