Canonical Allele Identifier: CA1167986531
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063508G= , CM000663.2:g.55063508G= GRCh38
NC_000001.10:g.55529181G= , CM000663.1:g.55529181G= GRCh37
NC_000001.9:g.55301769G= NCBI36
NG_009061.1:g.28962G= , LRG_275:g.28962G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*343G= ENSP00000501161.2:n.*343G=
ENST00000710286.1:c.2360G= ENSP00000518176.1:p.Ser787=
ENST00000673903.1:c.1628G= ENSP00000501257.1:p.Ser543=
ENST00000673913.1:c.853G= ENSP00000501161.1:n.853G=
ENST00000302118.5:c.2003G= MANE Select ENSP00000303208.5:p.Ser668=
ENST00000490692.1:n.2549G=
NM_174936.3:c.2003G= , LRG_275t1:c.2003G= NP_777596.2:p.Ser668=
NR_110451.1:n.1610G=
XM_011541193.1:c.1124G= XP_011539495.1:p.Ser375=
NM_174936.4:c.2003G= MANE Select NP_777596.2:p.Ser668=
NR_110451.2:n.1610G=