Canonical Allele Identifier: CA1167985704
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061468G= , CM000663.2:g.55061468G= GRCh38
NC_000001.10:g.55527141G= , CM000663.1:g.55527141G= GRCh37
NC_000001.9:g.55299729G= NCBI36
NG_009061.1:g.26922G= , LRG_275:g.26922G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*115G= ENSP00000501161.2:n.*115G=
ENST00000710286.1:c.2132G= ENSP00000518176.1:p.Arg711=
ENST00000673903.1:c.1400G= ENSP00000501257.1:p.Arg467=
ENST00000673913.1:c.625G= ENSP00000501161.1:n.625G=
ENST00000302118.5:c.1775G= MANE Select ENSP00000303208.5:p.Arg592=
ENST00000490692.1:n.2321G=
NM_174936.3:c.1775G= , LRG_275t1:c.1775G= NP_777596.2:p.Arg592=
NR_110451.1:n.1382G=
XM_011541193.1:c.896G= XP_011539495.1:p.Arg299=
NM_174936.4:c.1775G= MANE Select NP_777596.2:p.Arg592=
NR_110451.2:n.1382G=