Canonical Allele Identifier: CA1167984901
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059533T= , CM000663.2:g.55059533T= GRCh38
NC_000001.10:g.55525206T= , CM000663.1:g.55525206T= GRCh37
NC_000001.9:g.55297794T= NCBI36
NG_009061.1:g.24987T= , LRG_275:g.24987T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1551T= ENSP00000501161.2:p.Gly517=
ENST00000710286.1:c.1908T= ENSP00000518176.1:p.Gly636=
ENST00000673903.1:c.1176T= ENSP00000501257.1:p.Gly392=
ENST00000673913.1:c.291T= ENSP00000501161.1:p.Gly97=
ENST00000302118.5:c.1551T= MANE Select ENSP00000303208.5:p.Gly517=
ENST00000490692.1:n.2227+886T=
NM_174936.3:c.1551T= , LRG_275t1:c.1551T= NP_777596.2:p.Gly517=
NR_110451.1:n.1158T=
XM_011541193.1:c.672T= XP_011539495.1:p.Gly224=
NM_174936.4:c.1551T= MANE Select NP_777596.2:p.Gly517=
NR_110451.2:n.1158T=