Canonical Allele Identifier: CA1141809056
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55058549C= , CM000663.2:g.55058549C= GRCh38
NC_000001.10:g.55524222C= , CM000663.1:g.55524222C= GRCh37
NC_000001.9:g.55296810C= NCBI36
NG_009061.1:g.24003C= , LRG_275:g.24003C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1405C= ENSP00000501161.2:p.Arg469=
ENST00000710286.1:c.1762C= ENSP00000518176.1:p.Arg588=
ENST00000673903.1:c.1030C= ENSP00000501257.1:p.Arg344=
ENST00000673913.1:c.145C= ENSP00000501161.1:p.Arg49=
ENST00000302118.5:c.1405C= MANE Select ENSP00000303208.5:p.Arg469=
ENST00000490692.1:n.2129C=
NM_174936.3:c.1405C= , LRG_275t1:c.1405C= NP_777596.2:p.Arg469=
NR_110451.1:n.1012C=
XM_011541193.1:c.526C= XP_011539495.1:p.Arg176=
NM_174936.4:c.1405C= MANE Select NP_777596.2:p.Arg469=
NR_110451.2:n.1012C=