Canonical Allele Identifier: CA1167986559
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063563G= , CM000663.2:g.55063563G= GRCh38
NC_000001.10:g.55529236G= , CM000663.1:g.55529236G= GRCh37
NC_000001.9:g.55301824G= NCBI36
NG_009061.1:g.29017G= , LRG_275:g.29017G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*398G= ENSP00000501161.2:n.*398G=
ENST00000710286.1:c.2415G= ENSP00000518176.1:p.Gln805=
ENST00000673903.1:c.1683G= ENSP00000501257.1:p.Gln561=
ENST00000302118.5:c.2058G= MANE Select ENSP00000303208.5:p.Gln686=
ENST00000490692.1:n.2604G=
NM_174936.3:c.2058G= , LRG_275t1:c.2058G= NP_777596.2:p.Gln686=
NR_110451.1:n.1665G=
XM_011541193.1:c.1179G= XP_011539495.1:p.Gln393=
NM_174936.4:c.2058G= MANE Select NP_777596.2:p.Gln686=
NR_110451.2:n.1665G=