Canonical Allele Identifier: CA1167985710
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061486C= , CM000663.2:g.55061486C= GRCh38
NC_000001.10:g.55527159C= , CM000663.1:g.55527159C= GRCh37
NC_000001.9:g.55299747C= NCBI36
NG_009061.1:g.26940C= , LRG_275:g.26940C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*133C= ENSP00000501161.2:n.*133C=
ENST00000710286.1:c.2150C= ENSP00000518176.1:p.Ala717=
ENST00000673903.1:c.1418C= ENSP00000501257.1:p.Ala473=
ENST00000673913.1:c.643C= ENSP00000501161.1:n.643C=
ENST00000302118.5:c.1793C= MANE Select ENSP00000303208.5:p.Ala598=
ENST00000490692.1:n.2339C=
NM_174936.3:c.1793C= , LRG_275t1:c.1793C= NP_777596.2:p.Ala598=
NR_110451.1:n.1400C=
XM_011541193.1:c.914C= XP_011539495.1:p.Ala305=
NM_174936.4:c.1793C= MANE Select NP_777596.2:p.Ala598=
NR_110451.2:n.1400C=