Canonical Allele Identifier: CA1167984927
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059613C= , CM000663.2:g.55059613C= GRCh38
NC_000001.10:g.55525286C= , CM000663.1:g.55525286C= GRCh37
NC_000001.9:g.55297874C= NCBI36
NG_009061.1:g.25067C= , LRG_275:g.25067C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1631C= ENSP00000501161.2:p.Ala544=
ENST00000710286.1:c.1988C= ENSP00000518176.1:p.Ala663=
ENST00000673903.1:c.1256C= ENSP00000501257.1:p.Ala419=
ENST00000673913.1:c.371C= ENSP00000501161.1:p.Ala124=
ENST00000302118.5:c.1631C= MANE Select ENSP00000303208.5:p.Ala544=
ENST00000490692.1:n.2227+966C=
NM_174936.3:c.1631C= , LRG_275t1:c.1631C= NP_777596.2:p.Ala544=
NR_110451.1:n.1238C=
XM_011541193.1:c.752C= XP_011539495.1:p.Ala251=
NM_174936.4:c.1631C= MANE Select NP_777596.2:p.Ala544=
NR_110451.2:n.1238C=