Canonical Allele Identifier: CA1167985725
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061526G= , CM000663.2:g.55061526G= GRCh38
NC_000001.10:g.55527199G= , CM000663.1:g.55527199G= GRCh37
NC_000001.9:g.55299787G= NCBI36
NG_009061.1:g.26980G= , LRG_275:g.26980G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*173G= ENSP00000501161.2:n.*173G=
ENST00000710286.1:c.2190G= ENSP00000518176.1:p.Lys730=
ENST00000673903.1:c.1458G= ENSP00000501257.1:p.Lys486=
ENST00000673913.1:c.683G= ENSP00000501161.1:n.683G=
ENST00000302118.5:c.1833G= MANE Select ENSP00000303208.5:p.Lys611=
ENST00000490692.1:n.2379G=
NM_174936.3:c.1833G= , LRG_275t1:c.1833G= NP_777596.2:p.Lys611=
NR_110451.1:n.1440G=
XM_011541193.1:c.954G= XP_011539495.1:p.Lys318=
NM_174936.4:c.1833G= MANE Select NP_777596.2:p.Lys611=
NR_110451.2:n.1440G=