Canonical Allele Identifier: CA340480558

Gene: PCSK9

Linked Data

• gnomAD v4: 1-55063378-G-A
• MyVariant Identifiers: chr1:g.55529051G>A (hg19) ; chr1:g.55063378G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55063378G>A , CM000663.2:g.55063378G>A	GRCh38
NC_000001.10:g.55529051G>A , CM000663.1:g.55529051G>A	GRCh37
NC_000001.9:g.55301639G>A	NCBI36
NG_009061.1:g.28832G>A , LRG_275:g.28832G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*213G>A	ENSP00000501161.2:n.*213G>A
ENST00000710286.1:c.2230G>A	ENSP00000518176.1:p.Ala744Thr
ENST00000673903.1:c.1498G>A	ENSP00000501257.1:p.Ala500Thr
ENST00000673913.1:c.723G>A	ENSP00000501161.1:n.723G>A
ENST00000302118.5:c.1873G>A MANE Select	ENSP00000303208.5:p.Ala625Thr
ENST00000490692.1:n.2419G>A
NM_174936.3:c.1873G>A , LRG_275t1:c.1873G>A	NP_777596.2:p.Ala625Thr
NR_110451.1:n.1480G>A
XM_011541193.1:c.994G>A	XP_011539495.1:p.Ala332Thr
NM_174936.4:c.1873G>A MANE Select	NP_777596.2:p.Ala625Thr
NR_110451.2:n.1480G>A