Canonical Allele Identifier: CA340479878

Gene: PCSK9

Linked Data

• gnomAD v4: 1-55059553-C-T
• MyVariant Identifiers: chr1:g.55525226C>T (hg19) ; chr1:g.55059553C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059553C>T , CM000663.2:g.55059553C>T	GRCh38
NC_000001.10:g.55525226C>T , CM000663.1:g.55525226C>T	GRCh37
NC_000001.9:g.55297814C>T	NCBI36
NG_009061.1:g.25007C>T , LRG_275:g.25007C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1571C>T	ENSP00000501161.2:p.Ala524Val
ENST00000710286.1:c.1928C>T	ENSP00000518176.1:p.Ala643Val
ENST00000673903.1:c.1196C>T	ENSP00000501257.1:p.Ala399Val
ENST00000673913.1:c.311C>T	ENSP00000501161.1:p.Ala104Val
ENST00000302118.5:c.1571C>T MANE Select	ENSP00000303208.5:p.Ala524Val
ENST00000490692.1:n.2227+906C>T
NM_174936.3:c.1571C>T , LRG_275t1:c.1571C>T	NP_777596.2:p.Ala524Val
NR_110451.1:n.1178C>T
XM_011541193.1:c.692C>T	XP_011539495.1:p.Ala231Val
NM_174936.4:c.1571C>T MANE Select	NP_777596.2:p.Ala524Val
NR_110451.2:n.1178C>T