Canonical Allele Identifier: CA1167985755
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061586G= , CM000663.2:g.55061586G= GRCh38
NC_000001.10:g.55527259G= , CM000663.1:g.55527259G= GRCh37
NC_000001.9:g.55299847G= NCBI36
NG_009061.1:g.27040G= , LRG_275:g.27040G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*203+30G= ENSP00000501161.2:n.*203+30G=
ENST00000710286.1:c.2220+30G= ENSP00000518176.1:n.2220+30G=
ENST00000673903.1:c.1488+30G= ENSP00000501257.1:n.1488+30G=
ENST00000673913.1:c.713+30G= ENSP00000501161.1:n.713+30G=
ENST00000302118.5:c.1863+30G= MANE Select ENSP00000303208.5:n.1863+30G=
ENST00000490692.1:n.2409+30G=
NM_174936.3:c.1863+30G= , LRG_275t1:c.1863+30G= NP_777596.2:n.1863+30G=
NR_110451.1:n.1470+30G=
XM_011541193.1:c.984+30G= XP_011539495.1:n.984+30G=
NM_174936.4:c.1863+30G= MANE Select NP_777596.2:n.1863+30G=
NR_110451.2:n.1470+30G=