Canonical Allele Identifier: CA1167985730
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061531A= , CM000663.2:g.55061531A= GRCh38
NC_000001.10:g.55527204A= , CM000663.1:g.55527204A= GRCh37
NC_000001.9:g.55299792A= NCBI36
NG_009061.1:g.26985A= , LRG_275:g.26985A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*178A= ENSP00000501161.2:n.*178A=
ENST00000710286.1:c.2195A= ENSP00000518176.1:p.His732=
ENST00000673903.1:c.1463A= ENSP00000501257.1:p.His488=
ENST00000673913.1:c.688A= ENSP00000501161.1:n.688A=
ENST00000302118.5:c.1838A= MANE Select ENSP00000303208.5:p.His613=
ENST00000490692.1:n.2384A=
NM_174936.3:c.1838A= , LRG_275t1:c.1838A= NP_777596.2:p.His613=
NR_110451.1:n.1445A=
XM_011541193.1:c.959A= XP_011539495.1:p.His320=
NM_174936.4:c.1838A= MANE Select NP_777596.2:p.His613=
NR_110451.2:n.1445A=