Canonical Allele Identifier: CA1167985720
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061506G= , CM000663.2:g.55061506G= GRCh38
NC_000001.10:g.55527179G= , CM000663.1:g.55527179G= GRCh37
NC_000001.9:g.55299767G= NCBI36
NG_009061.1:g.26960G= , LRG_275:g.26960G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*153G= ENSP00000501161.2:n.*153G=
ENST00000710286.1:c.2170G= ENSP00000518176.1:p.Gly724=
ENST00000673903.1:c.1438G= ENSP00000501257.1:p.Gly480=
ENST00000673913.1:c.663G= ENSP00000501161.1:n.663G=
ENST00000302118.5:c.1813G= MANE Select ENSP00000303208.5:p.Gly605=
ENST00000490692.1:n.2359G=
NM_174936.3:c.1813G= , LRG_275t1:c.1813G= NP_777596.2:p.Gly605=
NR_110451.1:n.1420G=
XM_011541193.1:c.934G= XP_011539495.1:p.Gly312=
NM_174936.4:c.1813G= MANE Select NP_777596.2:p.Gly605=
NR_110451.2:n.1420G=