Canonical Allele Identifier: CA1167984862
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059460T= , CM000663.2:g.55059460T= GRCh38
NC_000001.10:g.55525133T= , CM000663.1:g.55525133T= GRCh37
NC_000001.9:g.55297721T= NCBI36
NG_009061.1:g.24914T= , LRG_275:g.24914T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1504-26T= ENSP00000501161.2:n.1504-26T=
ENST00000710286.1:c.1861-26T= ENSP00000518176.1:n.1861-26T=
ENST00000673903.1:c.1129-26T= ENSP00000501257.1:n.1129-26T=
ENST00000673913.1:c.244-26T= ENSP00000501161.1:n.244-26T=
ENST00000302118.5:c.1504-26T= MANE Select ENSP00000303208.5:n.1504-26T=
ENST00000490692.1:n.2227+813T=
NM_174936.3:c.1504-26T= , LRG_275t1:c.1504-26T= NP_777596.2:n.1504-26T=
NR_110451.1:n.1111-26T=
XM_011541193.1:c.625-26T= XP_011539495.1:n.625-26T=
NM_174936.4:c.1504-26T= MANE Select NP_777596.2:n.1504-26T=
NR_110451.2:n.1111-26T=