Canonical Allele Identifier: CA1167984944
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059654G= , CM000663.2:g.55059654G= GRCh38
NC_000001.10:g.55525327G= , CM000663.1:g.55525327G= GRCh37
NC_000001.9:g.55297915G= NCBI36
NG_009061.1:g.25108G= , LRG_275:g.25108G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1672G= ENSP00000501161.2:p.Val558=
ENST00000710286.1:c.2029G= ENSP00000518176.1:p.Val677=
ENST00000673903.1:c.1297G= ENSP00000501257.1:p.Val433=
ENST00000673913.1:c.412G= ENSP00000501161.1:p.Val138=
ENST00000302118.5:c.1672G= MANE Select ENSP00000303208.5:p.Val558=
ENST00000490692.1:n.2227+1007G=
NM_174936.3:c.1672G= , LRG_275t1:c.1672G= NP_777596.2:p.Val558=
NR_110451.1:n.1279G=
XM_011541193.1:c.793G= XP_011539495.1:p.Val265=
NM_174936.4:c.1672G= MANE Select NP_777596.2:p.Val558=
NR_110451.2:n.1279G=