Canonical Allele Identifier: CA1167986515
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063466G= , CM000663.2:g.55063466G= GRCh38
NC_000001.10:g.55529139G= , CM000663.1:g.55529139G= GRCh37
NC_000001.9:g.55301727G= NCBI36
NG_009061.1:g.28920G= , LRG_275:g.28920G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*301G= ENSP00000501161.2:n.*301G=
ENST00000710286.1:c.2318G= ENSP00000518176.1:p.Cys773=
ENST00000673903.1:c.1586G= ENSP00000501257.1:p.Cys529=
ENST00000673913.1:c.811G= ENSP00000501161.1:n.811G=
ENST00000302118.5:c.1961G= MANE Select ENSP00000303208.5:p.Cys654=
ENST00000490692.1:n.2507G=
NM_174936.3:c.1961G= , LRG_275t1:c.1961G= NP_777596.2:p.Cys654=
NR_110451.1:n.1568G=
XM_011541193.1:c.1082G= XP_011539495.1:p.Cys361=
NM_174936.4:c.1961G= MANE Select NP_777596.2:p.Cys654=
NR_110451.2:n.1568G=