Canonical Allele Identifier: CA1167985005
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059779G= , CM000663.2:g.55059779G= GRCh38
NC_000001.10:g.55525452G= , CM000663.1:g.55525452G= GRCh37
NC_000001.9:g.55298040G= NCBI36
NG_009061.1:g.25233G= , LRG_275:g.25233G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1681+116G= ENSP00000501161.2:n.1681+116G=
ENST00000710286.1:c.2038+116G= ENSP00000518176.1:n.2038+116G=
ENST00000673903.1:c.1306+116G= ENSP00000501257.1:n.1306+116G=
ENST00000673913.1:c.421+116G= ENSP00000501161.1:n.421+116G=
ENST00000302118.5:c.1681+116G= MANE Select ENSP00000303208.5:n.1681+116G=
ENST00000490692.1:n.2227+1132G=
NM_174936.3:c.1681+116G= , LRG_275t1:c.1681+116G= NP_777596.2:n.1681+116G=
NR_110451.1:n.1288+116G=
XM_011541193.1:c.802+116G= XP_011539495.1:n.802+116G=
NM_174936.4:c.1681+116G= MANE Select NP_777596.2:n.1681+116G=
NR_110451.2:n.1288+116G=