Canonical Allele Identifier: CA1167984824
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059355C= , CM000663.2:g.55059355C= GRCh38
NC_000001.10:g.55525028C= , CM000663.1:g.55525028C= GRCh37
NC_000001.9:g.55297616C= NCBI36
NG_009061.1:g.24809C= , LRG_275:g.24809C=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.1504-131C= ENSP00000501161.2:n.1504-131C=
ENST00000710286.1:c.1861-131C= ENSP00000518176.1:n.1861-131C=
ENST00000673903.1:c.1129-131C= ENSP00000501257.1:n.1129-131C=
ENST00000673913.1:c.244-131C= ENSP00000501161.1:n.244-131C=
ENST00000302118.5:c.1504-131C= MANE Select ENSP00000303208.5:n.1504-131C=
ENST00000490692.1:n.2227+708C=
NM_174936.3:c.1504-131C= , LRG_275t1:c.1504-131C= NP_777596.2:n.1504-131C=
NR_110451.1:n.1111-131C=
XM_011541193.1:c.625-131C= XP_011539495.1:n.625-131C=
NM_174936.4:c.1504-131C= MANE Select NP_777596.2:n.1504-131C=
NR_110451.2:n.1111-131C=