Canonical Allele Identifier: CA1167985729
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061530C= , CM000663.2:g.55061530C= GRCh38
NC_000001.10:g.55527203C= , CM000663.1:g.55527203C= GRCh37
NC_000001.9:g.55299791C= NCBI36
NG_009061.1:g.26984C= , LRG_275:g.26984C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*177C= ENSP00000501161.2:n.*177C=
ENST00000710286.1:c.2194C= ENSP00000518176.1:p.His732=
ENST00000673903.1:c.1462C= ENSP00000501257.1:p.His488=
ENST00000673913.1:c.687C= ENSP00000501161.1:n.687C=
ENST00000302118.5:c.1837C= MANE Select ENSP00000303208.5:p.His613=
ENST00000490692.1:n.2383C=
NM_174936.3:c.1837C= , LRG_275t1:c.1837C= NP_777596.2:p.His613=
NR_110451.1:n.1444C=
XM_011541193.1:c.958C= XP_011539495.1:p.His320=
NM_174936.4:c.1837C= MANE Select NP_777596.2:p.His613=
NR_110451.2:n.1444C=