Canonical Allele Identifier: CA417960552

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55527175C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55061502C>A , CM000663.2:g.55061502C>A	GRCh38
NC_000001.10:g.55527175C>A , CM000663.1:g.55527175C>A	GRCh37
NC_000001.9:g.55299763C>A	NCBI36
NG_009061.1:g.26956C>A , LRG_275:g.26956C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*149C>A	ENSP00000501161.2:n.*149C>A
ENST00000710286.1:c.2166C>A	ENSP00000518176.1:p.Ala722=
ENST00000673903.1:c.1434C>A	ENSP00000501257.1:p.Ala478=
ENST00000673913.1:c.659C>A	ENSP00000501161.1:n.659C>A
ENST00000302118.5:c.1809C>A MANE Select	ENSP00000303208.5:p.Ala603=
ENST00000490692.1:n.2355C>A
NM_174936.3:c.1809C>A , LRG_275t1:c.1809C>A	NP_777596.2:p.Ala603=
NR_110451.1:n.1416C>A
XM_011541193.1:c.930C>A	XP_011539495.1:p.Ala310=
NM_174936.4:c.1809C>A MANE Select	NP_777596.2:p.Ala603=
NR_110451.2:n.1416C>A