Canonical Allele Identifier: CA1167984934
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059627C= , CM000663.2:g.55059627C= GRCh38
NC_000001.10:g.55525300C= , CM000663.1:g.55525300C= GRCh37
NC_000001.9:g.55297888C= NCBI36
NG_009061.1:g.25081C= , LRG_275:g.25081C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1645C= ENSP00000501161.2:p.Arg549=
ENST00000710286.1:c.2002C= ENSP00000518176.1:p.Arg668=
ENST00000673903.1:c.1270C= ENSP00000501257.1:p.Arg424=
ENST00000673913.1:c.385C= ENSP00000501161.1:p.Arg129=
ENST00000302118.5:c.1645C= MANE Select ENSP00000303208.5:p.Arg549=
ENST00000490692.1:n.2227+980C=
NM_174936.3:c.1645C= , LRG_275t1:c.1645C= NP_777596.2:p.Arg549=
NR_110451.1:n.1252C=
XM_011541193.1:c.766C= XP_011539495.1:p.Arg256=
NM_174936.4:c.1645C= MANE Select NP_777596.2:p.Arg549=
NR_110451.2:n.1252C=