Canonical Allele Identifier: CA1167985715
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061498A= , CM000663.2:g.55061498A= GRCh38
NC_000001.10:g.55527171A= , CM000663.1:g.55527171A= GRCh37
NC_000001.9:g.55299759A= NCBI36
NG_009061.1:g.26952A= , LRG_275:g.26952A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*145A= ENSP00000501161.2:n.*145A=
ENST00000710286.1:c.2162A= ENSP00000518176.1:p.His721=
ENST00000673903.1:c.1430A= ENSP00000501257.1:p.His477=
ENST00000673913.1:c.655A= ENSP00000501161.1:n.655A=
ENST00000302118.5:c.1805A= MANE Select ENSP00000303208.5:p.His602=
ENST00000490692.1:n.2351A=
NM_174936.3:c.1805A= , LRG_275t1:c.1805A= NP_777596.2:p.His602=
NR_110451.1:n.1412A=
XM_011541193.1:c.926A= XP_011539495.1:p.His309=
NM_174936.4:c.1805A= MANE Select NP_777596.2:p.His602=
NR_110451.2:n.1412A=