Canonical Allele Identifier: CA1167984929
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059618A= , CM000663.2:g.55059618A= GRCh38
NC_000001.10:g.55525291A= , CM000663.1:g.55525291A= GRCh37
NC_000001.9:g.55297879A= NCBI36
NG_009061.1:g.25072A= , LRG_275:g.25072A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1636A= ENSP00000501161.2:p.Met546=
ENST00000710286.1:c.1993A= ENSP00000518176.1:p.Met665=
ENST00000673903.1:c.1261A= ENSP00000501257.1:p.Met421=
ENST00000673913.1:c.376A= ENSP00000501161.1:p.Met126=
ENST00000302118.5:c.1636A= MANE Select ENSP00000303208.5:p.Met546=
ENST00000490692.1:n.2227+971A=
NM_174936.3:c.1636A= , LRG_275t1:c.1636A= NP_777596.2:p.Met546=
NR_110451.1:n.1243A=
XM_011541193.1:c.757A= XP_011539495.1:p.Met253=
NM_174936.4:c.1636A= MANE Select NP_777596.2:p.Met546=
NR_110451.2:n.1243A=