Canonical Allele Identifier: CA1167981516
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55052301T= , CM000663.2:g.55052301T= GRCh38
NC_000001.10:g.55517974T= , CM000663.1:g.55517974T= GRCh37
NC_000001.9:g.55290562T= NCBI36
NG_009061.1:g.17755T= , LRG_275:g.17755T=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.547T= ENSP00000501161.2:p.Tyr183=
ENST00000710286.1:c.904T= ENSP00000518176.1:p.Tyr302=
ENST00000673726.1:c.*43T= ENSP00000501004.1:n.*43T=
ENST00000673903.1:c.172T= ENSP00000501257.1:p.Tyr58=
ENST00000302118.5:c.547T= MANE Select ENSP00000303208.5:p.Tyr183=
ENST00000490692.1:n.1368T=
NM_174936.3:c.547T= , LRG_275t1:c.547T= NP_777596.2:p.Tyr183=
NR_110451.1:n.206T=
NM_174936.4:c.547T= MANE Select NP_777596.2:p.Tyr183=
NR_110451.2:n.206T=