Canonical Allele Identifier: CA340480427

Gene: PCSK9

Linked Data

• gnomAD v4: 1-55061507-G-T
• MyVariant Identifiers: chr1:g.55527180G>T (hg19) ; chr1:g.55061507G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.55061507G>T , CM000663.2:g.55061507G>T	GRCh38
NC_000001.10:g.55527180G>T , CM000663.1:g.55527180G>T	GRCh37
NC_000001.9:g.55299768G>T	NCBI36
NG_009061.1:g.26961G>T , LRG_275:g.26961G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000673913.2:c.*154G>T	ENSP00000501161.2:n.*154G>T
ENST00000710286.1:c.2171G>T	ENSP00000518176.1:p.Gly724Val
ENST00000673903.1:c.1439G>T	ENSP00000501257.1:p.Gly480Val
ENST00000673913.1:c.664G>T	ENSP00000501161.1:n.664G>T
ENST00000302118.5:c.1814G>T MANE Select	ENSP00000303208.5:p.Gly605Val
ENST00000490692.1:n.2360G>T
NM_174936.3:c.1814G>T , LRG_275t1:c.1814G>T	NP_777596.2:p.Gly605Val
NR_110451.1:n.1421G>T
XM_011541193.1:c.935G>T	XP_011539495.1:p.Gly312Val
NM_174936.4:c.1814G>T MANE Select	NP_777596.2:p.Gly605Val
NR_110451.2:n.1421G>T