Canonical Allele Identifier: CA1167986524
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063492A= , CM000663.2:g.55063492A= GRCh38
NC_000001.10:g.55529165A= , CM000663.1:g.55529165A= GRCh37
NC_000001.9:g.55301753A= NCBI36
NG_009061.1:g.28946A= , LRG_275:g.28946A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*327A= ENSP00000501161.2:n.*327A=
ENST00000710286.1:c.2344A= ENSP00000518176.1:p.Thr782=
ENST00000673903.1:c.1612A= ENSP00000501257.1:p.Thr538=
ENST00000673913.1:c.837A= ENSP00000501161.1:n.837A=
ENST00000302118.5:c.1987A= MANE Select ENSP00000303208.5:p.Thr663=
ENST00000490692.1:n.2533A=
NM_174936.3:c.1987A= , LRG_275t1:c.1987A= NP_777596.2:p.Thr663=
NR_110451.1:n.1594A=
XM_011541193.1:c.1108A= XP_011539495.1:p.Thr370=
NM_174936.4:c.1987A= MANE Select NP_777596.2:p.Thr663=
NR_110451.2:n.1594A=