Canonical Allele Identifier: CA1167986461
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063337A= , CM000663.2:g.55063337A= GRCh38
NC_000001.10:g.55529010A= , CM000663.1:g.55529010A= GRCh37
NC_000001.9:g.55301598A= NCBI36
NG_009061.1:g.28791A= , LRG_275:g.28791A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*204-32A= ENSP00000501161.2:n.*204-32A=
ENST00000710286.1:c.2221-32A= ENSP00000518176.1:n.2221-32A=
ENST00000673903.1:c.1489-32A= ENSP00000501257.1:n.1489-32A=
ENST00000673913.1:c.714-32A= ENSP00000501161.1:n.714-32A=
ENST00000302118.5:c.1864-32A= MANE Select ENSP00000303208.5:n.1864-32A=
ENST00000490692.1:n.2410-32A=
NM_174936.3:c.1864-32A= , LRG_275t1:c.1864-32A= NP_777596.2:n.1864-32A=
NR_110451.1:n.1471-32A=
XM_011541193.1:c.985-32A= XP_011539495.1:n.985-32A=
NM_174936.4:c.1864-32A= MANE Select NP_777596.2:n.1864-32A=
NR_110451.2:n.1471-32A=