Canonical Allele Identifier: CA1167984897
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059527T= , CM000663.2:g.55059527T= GRCh38
NC_000001.10:g.55525200T= , CM000663.1:g.55525200T= GRCh37
NC_000001.9:g.55297788T= NCBI36
NG_009061.1:g.24981T= , LRG_275:g.24981T=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.1545T= ENSP00000501161.2:p.Phe515=
ENST00000710286.1:c.1902T= ENSP00000518176.1:p.Phe634=
ENST00000673903.1:c.1170T= ENSP00000501257.1:p.Phe390=
ENST00000673913.1:c.285T= ENSP00000501161.1:p.Phe95=
ENST00000302118.5:c.1545T= MANE Select ENSP00000303208.5:p.Phe515=
ENST00000490692.1:n.2227+880T=
NM_174936.3:c.1545T= , LRG_275t1:c.1545T= NP_777596.2:p.Phe515=
NR_110451.1:n.1152T=
XM_011541193.1:c.666T= XP_011539495.1:p.Phe222=
NM_174936.4:c.1545T= MANE Select NP_777596.2:p.Phe515=
NR_110451.2:n.1152T=