Canonical Allele Identifier: CA1167985708
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061477G= , CM000663.2:g.55061477G= GRCh38
NC_000001.10:g.55527150G= , CM000663.1:g.55527150G= GRCh37
NC_000001.9:g.55299738G= NCBI36
NG_009061.1:g.26931G= , LRG_275:g.26931G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*124G= ENSP00000501161.2:n.*124G=
ENST00000710286.1:c.2141G= ENSP00000518176.1:p.Ser714=
ENST00000673903.1:c.1409G= ENSP00000501257.1:p.Ser470=
ENST00000673913.1:c.634G= ENSP00000501161.1:n.634G=
ENST00000302118.5:c.1784G= MANE Select ENSP00000303208.5:p.Ser595=
ENST00000490692.1:n.2330G=
NM_174936.3:c.1784G= , LRG_275t1:c.1784G= NP_777596.2:p.Ser595=
NR_110451.1:n.1391G=
XM_011541193.1:c.905G= XP_011539495.1:p.Ser302=
NM_174936.4:c.1784G= MANE Select NP_777596.2:p.Ser595=
NR_110451.2:n.1391G=