Canonical Allele Identifier: CA1167984427
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55058557C= , CM000663.2:g.55058557C= GRCh38
NC_000001.10:g.55524230C= , CM000663.1:g.55524230C= GRCh37
NC_000001.9:g.55296818C= NCBI36
NG_009061.1:g.24011C= , LRG_275:g.24011C=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.1413C= ENSP00000501161.2:p.Ala471=
ENST00000710286.1:c.1770C= ENSP00000518176.1:p.Ala590=
ENST00000673903.1:c.1038C= ENSP00000501257.1:p.Ala346=
ENST00000673913.1:c.153C= ENSP00000501161.1:p.Ala51=
ENST00000302118.5:c.1413C= MANE Select ENSP00000303208.5:p.Ala471=
ENST00000490692.1:n.2137C=
NM_174936.3:c.1413C= , LRG_275t1:c.1413C= NP_777596.2:p.Ala471=
NR_110451.1:n.1020C=
XM_011541193.1:c.534C= XP_011539495.1:p.Ala178=
NM_174936.4:c.1413C= MANE Select NP_777596.2:p.Ala471=
NR_110451.2:n.1020C=