Canonical Allele Identifier: CA1167984886
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059506C= , CM000663.2:g.55059506C= GRCh38
NC_000001.10:g.55525179C= , CM000663.1:g.55525179C= GRCh37
NC_000001.9:g.55297767C= NCBI36
NG_009061.1:g.24960C= , LRG_275:g.24960C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1524C= ENSP00000501161.2:p.Val508=
ENST00000710286.1:c.1881C= ENSP00000518176.1:p.Val627=
ENST00000673903.1:c.1149C= ENSP00000501257.1:p.Val383=
ENST00000673913.1:c.264C= ENSP00000501161.1:p.Val88=
ENST00000302118.5:c.1524C= MANE Select ENSP00000303208.5:p.Val508=
ENST00000490692.1:n.2227+859C=
NM_174936.3:c.1524C= , LRG_275t1:c.1524C= NP_777596.2:p.Val508=
NR_110451.1:n.1131C=
XM_011541193.1:c.645C= XP_011539495.1:p.Val215=
NM_174936.4:c.1524C= MANE Select NP_777596.2:p.Val508=
NR_110451.2:n.1131C=