Canonical Allele Identifier: CA1167985711
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061487T= , CM000663.2:g.55061487T= GRCh38
NC_000001.10:g.55527160T= , CM000663.1:g.55527160T= GRCh37
NC_000001.9:g.55299748T= NCBI36
NG_009061.1:g.26941T= , LRG_275:g.26941T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*134T= ENSP00000501161.2:n.*134T=
ENST00000710286.1:c.2151T= ENSP00000518176.1:p.Ala717=
ENST00000673903.1:c.1419T= ENSP00000501257.1:p.Ala473=
ENST00000673913.1:c.644T= ENSP00000501161.1:n.644T=
ENST00000302118.5:c.1794T= MANE Select ENSP00000303208.5:p.Ala598=
ENST00000490692.1:n.2340T=
NM_174936.3:c.1794T= , LRG_275t1:c.1794T= NP_777596.2:p.Ala598=
NR_110451.1:n.1401T=
XM_011541193.1:c.915T= XP_011539495.1:p.Ala305=
NM_174936.4:c.1794T= MANE Select NP_777596.2:p.Ala598=
NR_110451.2:n.1401T=