Canonical Allele Identifier: CA1167986644
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063757T= , CM000663.2:g.55063757T= GRCh38
NC_000001.10:g.55529430T= , CM000663.1:g.55529430T= GRCh37
NC_000001.9:g.55302018T= NCBI36
NG_009061.1:g.29211T= , LRG_275:g.29211T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*592T= ENSP00000501161.2:n.*592T=
ENST00000710286.1:c.*173T= ENSP00000518176.1:n.*173T=
ENST00000673903.1:c.*173T= ENSP00000501257.1:n.*173T=
ENST00000302118.5:c.*173T= MANE Select ENSP00000303208.5:n.*173T=
ENST00000490692.1:n.2798T=
NM_174936.3:c.*173T= , LRG_275t1:c.*173T= NP_777596.2:n.*173T=
NR_110451.1:n.1859T=
XM_011541193.1:c.*173T= XP_011539495.1:n.*173T=
NM_174936.4:c.*173T= MANE Select NP_777596.2:n.*173T=
NR_110451.2:n.1859T=