Canonical Allele Identifier: CA417960702

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55529218G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55063545G>A , CM000663.2:g.55063545G>A	GRCh38
NC_000001.10:g.55529218G>A , CM000663.1:g.55529218G>A	GRCh37
NC_000001.9:g.55301806G>A	NCBI36
NG_009061.1:g.28999G>A , LRG_275:g.28999G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*380G>A	ENSP00000501161.2:n.*380G>A
ENST00000710286.1:c.2397G>A	ENSP00000518176.1:p.Arg799=
ENST00000673903.1:c.1665G>A	ENSP00000501257.1:p.Arg555=
ENST00000302118.5:c.2040G>A MANE Select	ENSP00000303208.5:p.Arg680=
ENST00000490692.1:n.2586G>A
NM_174936.3:c.2040G>A , LRG_275t1:c.2040G>A	NP_777596.2:p.Arg680=
NR_110451.1:n.1647G>A
XM_011541193.1:c.1161G>A	XP_011539495.1:p.Arg387=
NM_174936.4:c.2040G>A MANE Select	NP_777596.2:p.Arg680=
NR_110451.2:n.1647G>A