Canonical Allele Identifier: CA1167986562
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063572G= , CM000663.2:g.55063572G= GRCh38
NC_000001.10:g.55529245G= , CM000663.1:g.55529245G= GRCh37
NC_000001.9:g.55301833G= NCBI36
NG_009061.1:g.29026G= , LRG_275:g.29026G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*407G= ENSP00000501161.2:n.*407G=
ENST00000710286.1:c.2424G= ENSP00000518176.1:p.Gln808=
ENST00000673903.1:c.1692G= ENSP00000501257.1:p.Gln564=
ENST00000302118.5:c.2067G= MANE Select ENSP00000303208.5:p.Gln689=
ENST00000490692.1:n.2613G=
NM_174936.3:c.2067G= , LRG_275t1:c.2067G= NP_777596.2:p.Gln689=
NR_110451.1:n.1674G=
XM_011541193.1:c.1188G= XP_011539495.1:p.Gln396=
NM_174936.4:c.2067G= MANE Select NP_777596.2:p.Gln689=
NR_110451.2:n.1674G=