Canonical Allele Identifier: CA1167985714
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061494T= , CM000663.2:g.55061494T= GRCh38
NC_000001.10:g.55527167T= , CM000663.1:g.55527167T= GRCh37
NC_000001.9:g.55299755T= NCBI36
NG_009061.1:g.26948T= , LRG_275:g.26948T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*141T= ENSP00000501161.2:n.*141T=
ENST00000710286.1:c.2158T= ENSP00000518176.1:p.Cys720=
ENST00000673903.1:c.1426T= ENSP00000501257.1:p.Cys476=
ENST00000673913.1:c.651T= ENSP00000501161.1:n.651T=
ENST00000302118.5:c.1801T= MANE Select ENSP00000303208.5:p.Cys601=
ENST00000490692.1:n.2347T=
NM_174936.3:c.1801T= , LRG_275t1:c.1801T= NP_777596.2:p.Cys601=
NR_110451.1:n.1408T=
XM_011541193.1:c.922T= XP_011539495.1:p.Cys308=
NM_174936.4:c.1801T= MANE Select NP_777596.2:p.Cys601=
NR_110451.2:n.1408T=