Canonical Allele Identifier: CA1167984852
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059428T= , CM000663.2:g.55059428T= GRCh38
NC_000001.10:g.55525101T= , CM000663.1:g.55525101T= GRCh37
NC_000001.9:g.55297689T= NCBI36
NG_009061.1:g.24882T= , LRG_275:g.24882T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1504-58T= ENSP00000501161.2:n.1504-58T=
ENST00000710286.1:c.1861-58T= ENSP00000518176.1:n.1861-58T=
ENST00000673903.1:c.1129-58T= ENSP00000501257.1:n.1129-58T=
ENST00000673913.1:c.244-58T= ENSP00000501161.1:n.244-58T=
ENST00000302118.5:c.1504-58T= MANE Select ENSP00000303208.5:n.1504-58T=
ENST00000490692.1:n.2227+781T=
NM_174936.3:c.1504-58T= , LRG_275t1:c.1504-58T= NP_777596.2:n.1504-58T=
NR_110451.1:n.1111-58T=
XM_011541193.1:c.625-58T= XP_011539495.1:n.625-58T=
NM_174936.4:c.1504-58T= MANE Select NP_777596.2:n.1504-58T=
NR_110451.2:n.1111-58T=