Canonical Allele Identifier: CA1167984921
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059590C= , CM000663.2:g.55059590C= GRCh38
NC_000001.10:g.55525263C= , CM000663.1:g.55525263C= GRCh37
NC_000001.9:g.55297851C= NCBI36
NG_009061.1:g.25044C= , LRG_275:g.25044C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1608C= ENSP00000501161.2:p.Val536=
ENST00000710286.1:c.1965C= ENSP00000518176.1:p.Val655=
ENST00000673903.1:c.1233C= ENSP00000501257.1:p.Val411=
ENST00000673913.1:c.348C= ENSP00000501161.1:p.Val116=
ENST00000302118.5:c.1608C= MANE Select ENSP00000303208.5:p.Val536=
ENST00000490692.1:n.2227+943C=
NM_174936.3:c.1608C= , LRG_275t1:c.1608C= NP_777596.2:p.Val536=
NR_110451.1:n.1215C=
XM_011541193.1:c.729C= XP_011539495.1:p.Val243=
NM_174936.4:c.1608C= MANE Select NP_777596.2:p.Val536=
NR_110451.2:n.1215C=