Canonical Allele Identifier: CA1167985707
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061472G= , CM000663.2:g.55061472G= GRCh38
NC_000001.10:g.55527145G= , CM000663.1:g.55527145G= GRCh37
NC_000001.9:g.55299733G= NCBI36
NG_009061.1:g.26926G= , LRG_275:g.26926G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*119G= ENSP00000501161.2:n.*119G=
ENST00000710286.1:c.2136G= ENSP00000518176.1:p.Glu712=
ENST00000673903.1:c.1404G= ENSP00000501257.1:p.Glu468=
ENST00000673913.1:c.629G= ENSP00000501161.1:n.629G=
ENST00000302118.5:c.1779G= MANE Select ENSP00000303208.5:p.Glu593=
ENST00000490692.1:n.2325G=
NM_174936.3:c.1779G= , LRG_275t1:c.1779G= NP_777596.2:p.Glu593=
NR_110451.1:n.1386G=
XM_011541193.1:c.900G= XP_011539495.1:p.Glu300=
NM_174936.4:c.1779G= MANE Select NP_777596.2:p.Glu593=
NR_110451.2:n.1386G=