Canonical Allele Identifier: CA1167986563
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063573G= , CM000663.2:g.55063573G= GRCh38
NC_000001.10:g.55529246G= , CM000663.1:g.55529246G= GRCh37
NC_000001.9:g.55301834G= NCBI36
NG_009061.1:g.29027G= , LRG_275:g.29027G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*408G= ENSP00000501161.2:n.*408G=
ENST00000710286.1:c.2425G= ENSP00000518176.1:p.Glu809=
ENST00000673903.1:c.1693G= ENSP00000501257.1:p.Glu565=
ENST00000302118.5:c.2068G= MANE Select ENSP00000303208.5:p.Glu690=
ENST00000490692.1:n.2614G=
NM_174936.3:c.2068G= , LRG_275t1:c.2068G= NP_777596.2:p.Glu690=
NR_110451.1:n.1675G=
XM_011541193.1:c.1189G= XP_011539495.1:p.Glu397=
NM_174936.4:c.2068G= MANE Select NP_777596.2:p.Glu690=
NR_110451.2:n.1675G=