Canonical Allele Identifier: CA340479805

Gene: PCSK9

Linked Data

• gnomAD v4: 1-55059537-G-T
• MyVariant Identifiers: chr1:g.55525210G>T (hg19) ; chr1:g.55059537G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55059537G>T , CM000663.2:g.55059537G>T	GRCh38
NC_000001.10:g.55525210G>T , CM000663.1:g.55525210G>T	GRCh37
NC_000001.9:g.55297798G>T	NCBI36
NG_009061.1:g.24991G>T , LRG_275:g.24991G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.1555G>T	ENSP00000501161.2:p.Gly519Cys
ENST00000710286.1:c.1912G>T	ENSP00000518176.1:p.Gly638Cys
ENST00000673903.1:c.1180G>T	ENSP00000501257.1:p.Gly394Cys
ENST00000673913.1:c.295G>T	ENSP00000501161.1:p.Gly99Cys
ENST00000302118.5:c.1555G>T MANE Select	ENSP00000303208.5:p.Gly519Cys
ENST00000490692.1:n.2227+890G>T
NM_174936.3:c.1555G>T , LRG_275t1:c.1555G>T	NP_777596.2:p.Gly519Cys
NR_110451.1:n.1162G>T
XM_011541193.1:c.676G>T	XP_011539495.1:p.Gly226Cys
NM_174936.4:c.1555G>T MANE Select	NP_777596.2:p.Gly519Cys
NR_110451.2:n.1162G>T