Canonical Allele Identifier: CA1167978101
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55043868A= , CM000663.2:g.55043868A= GRCh38
NC_000001.10:g.55509541A= , CM000663.1:g.55509541A= GRCh37
NC_000001.9:g.55282129A= NCBI36
NG_009061.1:g.9322A= , LRG_275:g.9322A=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.233A= ENSP00000501161.2:p.Tyr78=
ENST00000710286.1:c.590A= ENSP00000518176.1:p.Tyr197=
ENST00000673726.1:c.233A= ENSP00000501004.1:p.Tyr78=
ENST00000673903.1:c.-143A= ENSP00000501257.1:n.-143A=
ENST00000302118.5:c.233A= MANE Select ENSP00000303208.5:p.Tyr78=
NM_174936.3:c.233A= , LRG_275t1:c.233A= NP_777596.2:p.Tyr78=
NR_110451.1:n.182+3465A=
NM_174936.4:c.233A= MANE Select NP_777596.2:p.Tyr78=
NR_110451.2:n.182+3465A=