Canonical Allele Identifier: CA1167984918
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059583G= , CM000663.2:g.55059583G= GRCh38
NC_000001.10:g.55525256G= , CM000663.1:g.55525256G= GRCh37
NC_000001.9:g.55297844G= NCBI36
NG_009061.1:g.25037G= , LRG_275:g.25037G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1601G= ENSP00000501161.2:p.Cys534=
ENST00000710286.1:c.1958G= ENSP00000518176.1:p.Cys653=
ENST00000673903.1:c.1226G= ENSP00000501257.1:p.Cys409=
ENST00000673913.1:c.341G= ENSP00000501161.1:p.Cys114=
ENST00000302118.5:c.1601G= MANE Select ENSP00000303208.5:p.Cys534=
ENST00000490692.1:n.2227+936G=
NM_174936.3:c.1601G= , LRG_275t1:c.1601G= NP_777596.2:p.Cys534=
NR_110451.1:n.1208G=
XM_011541193.1:c.722G= XP_011539495.1:p.Cys241=
NM_174936.4:c.1601G= MANE Select NP_777596.2:p.Cys534=
NR_110451.2:n.1208G=