Canonical Allele Identifier: CA1167984940
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059647G= , CM000663.2:g.55059647G= GRCh38
NC_000001.10:g.55525320G= , CM000663.1:g.55525320G= GRCh37
NC_000001.9:g.55297908G= NCBI36
NG_009061.1:g.25101G= , LRG_275:g.25101G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1665G= ENSP00000501161.2:p.Gln555=
ENST00000710286.1:c.2022G= ENSP00000518176.1:p.Gln674=
ENST00000673903.1:c.1290G= ENSP00000501257.1:p.Gln430=
ENST00000673913.1:c.405G= ENSP00000501161.1:p.Gln135=
ENST00000302118.5:c.1665G= MANE Select ENSP00000303208.5:p.Gln555=
ENST00000490692.1:n.2227+1000G=
NM_174936.3:c.1665G= , LRG_275t1:c.1665G= NP_777596.2:p.Gln555=
NR_110451.1:n.1272G=
XM_011541193.1:c.786G= XP_011539495.1:p.Gln262=
NM_174936.4:c.1665G= MANE Select NP_777596.2:p.Gln555=
NR_110451.2:n.1272G=