Canonical Allele Identifier: CA1167985724
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061520A= , CM000663.2:g.55061520A= GRCh38
NC_000001.10:g.55527193A= , CM000663.1:g.55527193A= GRCh37
NC_000001.9:g.55299781A= NCBI36
NG_009061.1:g.26974A= , LRG_275:g.26974A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*167A= ENSP00000501161.2:n.*167A=
ENST00000710286.1:c.2184A= ENSP00000518176.1:p.Lys728=
ENST00000673903.1:c.1452A= ENSP00000501257.1:p.Lys484=
ENST00000673913.1:c.677A= ENSP00000501161.1:n.677A=
ENST00000302118.5:c.1827A= MANE Select ENSP00000303208.5:p.Lys609=
ENST00000490692.1:n.2373A=
NM_174936.3:c.1827A= , LRG_275t1:c.1827A= NP_777596.2:p.Lys609=
NR_110451.1:n.1434A=
XM_011541193.1:c.948A= XP_011539495.1:p.Lys316=
NM_174936.4:c.1827A= MANE Select NP_777596.2:p.Lys609=
NR_110451.2:n.1434A=