Canonical Allele Identifier: CA1167981521
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55052312C= , CM000663.2:g.55052312C= GRCh38
NC_000001.10:g.55517985C= , CM000663.1:g.55517985C= GRCh37
NC_000001.9:g.55290573C= NCBI36
NG_009061.1:g.17766C= , LRG_275:g.17766C=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.558C= ENSP00000501161.2:p.Asp186=
ENST00000710286.1:c.915C= ENSP00000518176.1:p.Asp305=
ENST00000673726.1:c.*54C= ENSP00000501004.1:n.*54C=
ENST00000673903.1:c.183C= ENSP00000501257.1:p.Asp61=
ENST00000302118.5:c.558C= MANE Select ENSP00000303208.5:p.Asp186=
ENST00000490692.1:n.1379C=
NM_174936.3:c.558C= , LRG_275t1:c.558C= NP_777596.2:p.Asp186=
NR_110451.1:n.217C=
NM_174936.4:c.558C= MANE Select NP_777596.2:p.Asp186=
NR_110451.2:n.217C=