Canonical Allele Identifier: CA1140023836
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059602A= , CM000663.2:g.55059602A= GRCh38
NC_000001.10:g.55525275A= , CM000663.1:g.55525275A= GRCh37
NC_000001.9:g.55297863A= NCBI36
NG_009061.1:g.25056A= , LRG_275:g.25056A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1620A= ENSP00000501161.2:p.Pro540=
ENST00000710286.1:c.1977A= ENSP00000518176.1:p.Pro659=
ENST00000673903.1:c.1245A= ENSP00000501257.1:p.Pro415=
ENST00000673913.1:c.360A= ENSP00000501161.1:p.Pro120=
ENST00000302118.5:c.1620A= MANE Select ENSP00000303208.5:p.Pro540=
ENST00000490692.1:n.2227+955A=
NM_174936.3:c.1620A= , LRG_275t1:c.1620A= NP_777596.2:p.Pro540=
NR_110451.1:n.1227A=
XM_011541193.1:c.741A= XP_011539495.1:p.Pro247=
NM_174936.4:c.1620A= MANE Select NP_777596.2:p.Pro540=
NR_110451.2:n.1227A=