Canonical Allele Identifier: CA1167984893
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059520A= , CM000663.2:g.55059520A= GRCh38
NC_000001.10:g.55525193A= , CM000663.1:g.55525193A= GRCh37
NC_000001.9:g.55297781A= NCBI36
NG_009061.1:g.24974A= , LRG_275:g.24974A=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.1538A= ENSP00000501161.2:p.Asn513=
ENST00000710286.1:c.1895A= ENSP00000518176.1:p.Asn632=
ENST00000673903.1:c.1163A= ENSP00000501257.1:p.Asn388=
ENST00000673913.1:c.278A= ENSP00000501161.1:p.Asn93=
ENST00000302118.5:c.1538A= MANE Select ENSP00000303208.5:p.Asn513=
ENST00000490692.1:n.2227+873A=
NM_174936.3:c.1538A= , LRG_275t1:c.1538A= NP_777596.2:p.Asn513=
NR_110451.1:n.1145A=
XM_011541193.1:c.659A= XP_011539495.1:p.Asn220=
NM_174936.4:c.1538A= MANE Select NP_777596.2:p.Asn513=
NR_110451.2:n.1145A=