Canonical Allele Identifier: CA1167985718
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061502C= , CM000663.2:g.55061502C= GRCh38
NC_000001.10:g.55527175C= , CM000663.1:g.55527175C= GRCh37
NC_000001.9:g.55299763C= NCBI36
NG_009061.1:g.26956C= , LRG_275:g.26956C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*149C= ENSP00000501161.2:n.*149C=
ENST00000710286.1:c.2166C= ENSP00000518176.1:p.Ala722=
ENST00000673903.1:c.1434C= ENSP00000501257.1:p.Ala478=
ENST00000673913.1:c.659C= ENSP00000501161.1:n.659C=
ENST00000302118.5:c.1809C= MANE Select ENSP00000303208.5:p.Ala603=
ENST00000490692.1:n.2355C=
NM_174936.3:c.1809C= , LRG_275t1:c.1809C= NP_777596.2:p.Ala603=
NR_110451.1:n.1416C=
XM_011541193.1:c.930C= XP_011539495.1:p.Ala310=
NM_174936.4:c.1809C= MANE Select NP_777596.2:p.Ala603=
NR_110451.2:n.1416C=