Canonical Allele Identifier: CA1001929495

Gene: PCSK9

Linked Data

• dbSNP Id: rs1644616901
• gnomAD v3: 1-55044034-G-GAAAAAA
• gnomAD v4: 1-55044034-G-GAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55044034_55044035insAAAAAA , CM000663.2:g.55044034_55044035insAAAAAA	GRCh38
NC_000001.10:g.55509707_55509708insAAAAAA , CM000663.1:g.55509707_55509708insAAAAAA	GRCh37
NC_000001.9:g.55282295_55282296insAAAAAA	NCBI36
NG_009061.1:g.9488_9489insAAAAAA , LRG_275:g.9488_9489insAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.399_399+1insAAAAAA	ENSP00000501161.2:n.399_399+1insAAAAAA
ENST00000710286.1:c.756_756+1insAAAAAA	ENSP00000518176.1:n.756_756+1insAAAAAA
ENST00000673662.1:n.69_69+1insAAAAAA
ENST00000673726.1:c.399_399+1insAAAAAA	ENSP00000501004.1:n.399_399+1insAAAAAA
ENST00000673903.1:c.24_24+1insAAAAAA	ENSP00000501257.1:n.24_24+1insAAAAAA
ENST00000302118.5:c.399_399+1insAAAAAA MANE Select	ENSP00000303208.5:n.399_399+1insAAAAAA
NM_174936.3:c.399_399+1insAAAAAA , LRG_275t1:c.399_399+1insAAAAAA	NP_777596.2:n.399_399+1insAAAAAA
NR_110451.1:n.182+3631_182+3632insAAAAAA
NM_174936.4:c.399_399+1insAAAAAA MANE Select	NP_777596.2:n.399_399+1insAAAAAA
NR_110451.2:n.182+3631_182+3632insAAAAAA