Canonical Allele Identifier: CA1142090995
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061449A= , CM000663.2:g.55061449A= GRCh38
NC_000001.10:g.55527122A= , CM000663.1:g.55527122A= GRCh37
NC_000001.9:g.55299710A= NCBI36
NG_009061.1:g.26903A= , LRG_275:g.26903A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*96A= ENSP00000501161.2:n.*96A=
ENST00000710286.1:c.2113A= ENSP00000518176.1:p.Asn705=
ENST00000673903.1:c.1381A= ENSP00000501257.1:p.Asn461=
ENST00000673913.1:c.606A= ENSP00000501161.1:n.606A=
ENST00000302118.5:c.1756A= MANE Select ENSP00000303208.5:p.Asn586=
ENST00000490692.1:n.2302A=
NM_174936.3:c.1756A= , LRG_275t1:c.1756A= NP_777596.2:p.Asn586=
NR_110451.1:n.1363A=
XM_011541193.1:c.877A= XP_011539495.1:p.Asn293=
NM_174936.4:c.1756A= MANE Select NP_777596.2:p.Asn586=
NR_110451.2:n.1363A=