Canonical Allele Identifier: CA1167986452
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063327G= , CM000663.2:g.55063327G= GRCh38
NC_000001.10:g.55529000G= , CM000663.1:g.55529000G= GRCh37
NC_000001.9:g.55301588G= NCBI36
NG_009061.1:g.28781G= , LRG_275:g.28781G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*204-42G= ENSP00000501161.2:n.*204-42G=
ENST00000710286.1:c.2221-42G= ENSP00000518176.1:n.2221-42G=
ENST00000673903.1:c.1489-42G= ENSP00000501257.1:n.1489-42G=
ENST00000673913.1:c.714-42G= ENSP00000501161.1:n.714-42G=
ENST00000302118.5:c.1864-42G= MANE Select ENSP00000303208.5:n.1864-42G=
ENST00000490692.1:n.2410-42G=
NM_174936.3:c.1864-42G= , LRG_275t1:c.1864-42G= NP_777596.2:n.1864-42G=
NR_110451.1:n.1471-42G=
XM_011541193.1:c.985-42G= XP_011539495.1:n.985-42G=
NM_174936.4:c.1864-42G= MANE Select NP_777596.2:n.1864-42G=
NR_110451.2:n.1471-42G=