Canonical Allele Identifier: CA1139809151
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55058564G= , CM000663.2:g.55058564G= GRCh38
NC_000001.10:g.55524237G= , CM000663.1:g.55524237G= GRCh37
NC_000001.9:g.55296825G= NCBI36
NG_009061.1:g.24018G= , LRG_275:g.24018G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1420G= ENSP00000501161.2:p.Val474=
ENST00000710286.1:c.1777G= ENSP00000518176.1:p.Val593=
ENST00000673903.1:c.1045G= ENSP00000501257.1:p.Val349=
ENST00000673913.1:c.160G= ENSP00000501161.1:p.Val54=
ENST00000302118.5:c.1420G= MANE Select ENSP00000303208.5:p.Val474=
ENST00000490692.1:n.2144G=
NM_174936.3:c.1420G= , LRG_275t1:c.1420G= NP_777596.2:p.Val474=
NR_110451.1:n.1027G=
XM_011541193.1:c.541G= XP_011539495.1:p.Val181=
NM_174936.4:c.1420G= MANE Select NP_777596.2:p.Val474=
NR_110451.2:n.1027G=