Canonical Allele Identifier: CA340479940

Gene: PCSK9

Linked Data

• gnomAD v4: 1-55059577-C-A
• MyVariant Identifiers: chr1:g.55525250C>A (hg19) ; chr1:g.55059577C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059577C>A , CM000663.2:g.55059577C>A	GRCh38
NC_000001.10:g.55525250C>A , CM000663.1:g.55525250C>A	GRCh37
NC_000001.9:g.55297838C>A	NCBI36
NG_009061.1:g.25031C>A , LRG_275:g.25031C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1595C>A	ENSP00000501161.2:p.Ala532Asp
ENST00000710286.1:c.1952C>A	ENSP00000518176.1:p.Ala651Asp
ENST00000673903.1:c.1220C>A	ENSP00000501257.1:p.Ala407Asp
ENST00000673913.1:c.335C>A	ENSP00000501161.1:p.Ala112Asp
ENST00000302118.5:c.1595C>A MANE Select	ENSP00000303208.5:p.Ala532Asp
ENST00000490692.1:n.2227+930C>A
NM_174936.3:c.1595C>A , LRG_275t1:c.1595C>A	NP_777596.2:p.Ala532Asp
NR_110451.1:n.1202C>A
XM_011541193.1:c.716C>A	XP_011539495.1:p.Ala239Asp
NM_174936.4:c.1595C>A MANE Select	NP_777596.2:p.Ala532Asp
NR_110451.2:n.1202C>A