Canonical Allele Identifier: CA1167985703
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061465A= , CM000663.2:g.55061465A= GRCh38
NC_000001.10:g.55527138A= , CM000663.1:g.55527138A= GRCh37
NC_000001.9:g.55299726A= NCBI36
NG_009061.1:g.26919A= , LRG_275:g.26919A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*112A= ENSP00000501161.2:n.*112A=
ENST00000710286.1:c.2129A= ENSP00000518176.1:p.His710=
ENST00000673903.1:c.1397A= ENSP00000501257.1:p.His466=
ENST00000673913.1:c.622A= ENSP00000501161.1:n.622A=
ENST00000302118.5:c.1772A= MANE Select ENSP00000303208.5:p.His591=
ENST00000490692.1:n.2318A=
NM_174936.3:c.1772A= , LRG_275t1:c.1772A= NP_777596.2:p.His591=
NR_110451.1:n.1379A=
XM_011541193.1:c.893A= XP_011539495.1:p.His298=
NM_174936.4:c.1772A= MANE Select NP_777596.2:p.His591=
NR_110451.2:n.1379A=