Canonical Allele Identifier: CA1167984892
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059519A= , CM000663.2:g.55059519A= GRCh38
NC_000001.10:g.55525192A= , CM000663.1:g.55525192A= GRCh37
NC_000001.9:g.55297780A= NCBI36
NG_009061.1:g.24973A= , LRG_275:g.24973A=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.1537A= ENSP00000501161.2:p.Asn513=
ENST00000710286.1:c.1894A= ENSP00000518176.1:p.Asn632=
ENST00000673903.1:c.1162A= ENSP00000501257.1:p.Asn388=
ENST00000673913.1:c.277A= ENSP00000501161.1:p.Asn93=
ENST00000302118.5:c.1537A= MANE Select ENSP00000303208.5:p.Asn513=
ENST00000490692.1:n.2227+872A=
NM_174936.3:c.1537A= , LRG_275t1:c.1537A= NP_777596.2:p.Asn513=
NR_110451.1:n.1144A=
XM_011541193.1:c.658A= XP_011539495.1:p.Asn220=
NM_174936.4:c.1537A= MANE Select NP_777596.2:p.Asn513=
NR_110451.2:n.1144A=