Canonical Allele Identifier: CA1167985739
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061553G= , CM000663.2:g.55061553G= GRCh38
NC_000001.10:g.55527226G= , CM000663.1:g.55527226G= GRCh37
NC_000001.9:g.55299814G= NCBI36
NG_009061.1:g.27007G= , LRG_275:g.27007G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*200G= ENSP00000501161.2:n.*200G=
ENST00000710286.1:c.2217G= ENSP00000518176.1:p.Glu739=
ENST00000673903.1:c.1485G= ENSP00000501257.1:p.Glu495=
ENST00000673913.1:c.710G= ENSP00000501161.1:n.710G=
ENST00000302118.5:c.1860G= MANE Select ENSP00000303208.5:p.Glu620=
ENST00000490692.1:n.2406G=
NM_174936.3:c.1860G= , LRG_275t1:c.1860G= NP_777596.2:p.Glu620=
NR_110451.1:n.1467G=
XM_011541193.1:c.981G= XP_011539495.1:p.Glu327=
NM_174936.4:c.1860G= MANE Select NP_777596.2:p.Glu620=
NR_110451.2:n.1467G=