Canonical Allele Identifier: CA340480328

Gene: PCSK9

Linked Data

• MyVariant Identifiers: chr1:g.55527135G>T (hg19) ; chr1:g.55061462G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55061462G>T , CM000663.2:g.55061462G>T	GRCh38
NC_000001.10:g.55527135G>T , CM000663.1:g.55527135G>T	GRCh37
NC_000001.9:g.55299723G>T	NCBI36
NG_009061.1:g.26916G>T , LRG_275:g.26916G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*109G>T	ENSP00000501161.2:n.*109G>T
ENST00000710286.1:c.2126G>T	ENSP00000518176.1:p.Gly709Val
ENST00000673903.1:c.1394G>T	ENSP00000501257.1:p.Gly465Val
ENST00000673913.1:c.619G>T	ENSP00000501161.1:n.619G>T
ENST00000302118.5:c.1769G>T MANE Select	ENSP00000303208.5:p.Gly590Val
ENST00000490692.1:n.2315G>T
NM_174936.3:c.1769G>T , LRG_275t1:c.1769G>T	NP_777596.2:p.Gly590Val
NR_110451.1:n.1376G>T
XM_011541193.1:c.890G>T	XP_011539495.1:p.Gly297Val
NM_174936.4:c.1769G>T MANE Select	NP_777596.2:p.Gly590Val
NR_110451.2:n.1376G>T