Canonical Allele Identifier: CA1167986668
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063810C= , CM000663.2:g.55063810C= GRCh38
NC_000001.10:g.55529483C= , CM000663.1:g.55529483C= GRCh37
NC_000001.9:g.55302071C= NCBI36
NG_009061.1:g.29264C= , LRG_275:g.29264C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*645C= ENSP00000501161.2:n.*645C=
ENST00000710286.1:c.*226C= ENSP00000518176.1:n.*226C=
ENST00000673903.1:c.*226C= ENSP00000501257.1:n.*226C=
ENST00000302118.5:c.*226C= MANE Select ENSP00000303208.5:n.*226C=
ENST00000490692.1:n.2851C=
NM_174936.3:c.*226C= , LRG_275t1:c.*226C= NP_777596.2:n.*226C=
NR_110451.1:n.1912C=
XM_011541193.1:c.*226C= XP_011539495.1:n.*226C=
NM_174936.4:c.*226C= MANE Select NP_777596.2:n.*226C=
NR_110451.2:n.1912C=