Canonical Allele Identifier: CA1143871923
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061458G= , CM000663.2:g.55061458G= GRCh38
NC_000001.10:g.55527131G= , CM000663.1:g.55527131G= GRCh37
NC_000001.9:g.55299719G= NCBI36
NG_009061.1:g.26912G= , LRG_275:g.26912G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*105G= ENSP00000501161.2:n.*105G=
ENST00000710286.1:c.2122G= ENSP00000518176.1:p.Val708=
ENST00000673903.1:c.1390G= ENSP00000501257.1:p.Val464=
ENST00000673913.1:c.615G= ENSP00000501161.1:n.615G=
ENST00000302118.5:c.1765G= MANE Select ENSP00000303208.5:p.Val589=
ENST00000490692.1:n.2311G=
NM_174936.3:c.1765G= , LRG_275t1:c.1765G= NP_777596.2:p.Val589=
NR_110451.1:n.1372G=
XM_011541193.1:c.886G= XP_011539495.1:p.Val296=
NM_174936.4:c.1765G= MANE Select NP_777596.2:p.Val589=
NR_110451.2:n.1372G=