Canonical Allele Identifier: CA1146549144
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063755C= , CM000663.2:g.55063755C= GRCh38
NC_000001.10:g.55529428C= , CM000663.1:g.55529428C= GRCh37
NC_000001.9:g.55302016C= NCBI36
NG_009061.1:g.29209C= , LRG_275:g.29209C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*590C= ENSP00000501161.2:n.*590C=
ENST00000710286.1:c.*171C= ENSP00000518176.1:n.*171C=
ENST00000673903.1:c.*171C= ENSP00000501257.1:n.*171C=
ENST00000302118.5:c.*171C= MANE Select ENSP00000303208.5:n.*171C=
ENST00000490692.1:n.2796C=
NM_174936.3:c.*171C= , LRG_275t1:c.*171C= NP_777596.2:n.*171C=
NR_110451.1:n.1857C=
XM_011541193.1:c.*171C= XP_011539495.1:n.*171C=
NM_174936.4:c.*171C= MANE Select NP_777596.2:n.*171C=
NR_110451.2:n.1857C=