Canonical Allele Identifier: CA1144436464
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061466C= , CM000663.2:g.55061466C= GRCh38
NC_000001.10:g.55527139C= , CM000663.1:g.55527139C= GRCh37
NC_000001.9:g.55299727C= NCBI36
NG_009061.1:g.26920C= , LRG_275:g.26920C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*113C= ENSP00000501161.2:n.*113C=
ENST00000710286.1:c.2130C= ENSP00000518176.1:p.His710=
ENST00000673903.1:c.1398C= ENSP00000501257.1:p.His466=
ENST00000673913.1:c.623C= ENSP00000501161.1:n.623C=
ENST00000302118.5:c.1773C= MANE Select ENSP00000303208.5:p.His591=
ENST00000490692.1:n.2319C=
NM_174936.3:c.1773C= , LRG_275t1:c.1773C= NP_777596.2:p.His591=
NR_110451.1:n.1380C=
XM_011541193.1:c.894C= XP_011539495.1:p.His298=
NM_174936.4:c.1773C= MANE Select NP_777596.2:p.His591=
NR_110451.2:n.1380C=