Canonical Allele Identifier: CA1167986556
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063559C= , CM000663.2:g.55063559C= GRCh38
NC_000001.10:g.55529232C= , CM000663.1:g.55529232C= GRCh37
NC_000001.9:g.55301820C= NCBI36
NG_009061.1:g.29013C= , LRG_275:g.29013C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*394C= ENSP00000501161.2:n.*394C=
ENST00000710286.1:c.2411C= ENSP00000518176.1:p.Ala804=
ENST00000673903.1:c.1679C= ENSP00000501257.1:p.Ala560=
ENST00000302118.5:c.2054C= MANE Select ENSP00000303208.5:p.Ala685=
ENST00000490692.1:n.2600C=
NM_174936.3:c.2054C= , LRG_275t1:c.2054C= NP_777596.2:p.Ala685=
NR_110451.1:n.1661C=
XM_011541193.1:c.1175C= XP_011539495.1:p.Ala392=
NM_174936.4:c.2054C= MANE Select NP_777596.2:p.Ala685=
NR_110451.2:n.1661C=