Canonical Allele Identifier: CA1167984859
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059458G= , CM000663.2:g.55059458G= GRCh38
NC_000001.10:g.55525131G= , CM000663.1:g.55525131G= GRCh37
NC_000001.9:g.55297719G= NCBI36
NG_009061.1:g.24912G= , LRG_275:g.24912G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1504-28G= ENSP00000501161.2:n.1504-28G=
ENST00000710286.1:c.1861-28G= ENSP00000518176.1:n.1861-28G=
ENST00000673903.1:c.1129-28G= ENSP00000501257.1:n.1129-28G=
ENST00000673913.1:c.244-28G= ENSP00000501161.1:n.244-28G=
ENST00000302118.5:c.1504-28G= MANE Select ENSP00000303208.5:n.1504-28G=
ENST00000490692.1:n.2227+811G=
NM_174936.3:c.1504-28G= , LRG_275t1:c.1504-28G= NP_777596.2:n.1504-28G=
NR_110451.1:n.1111-28G=
XM_011541193.1:c.625-28G= XP_011539495.1:n.625-28G=
NM_174936.4:c.1504-28G= MANE Select NP_777596.2:n.1504-28G=
NR_110451.2:n.1111-28G=
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