Canonical Allele Identifier: CA1167981888
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55053183G= , CM000663.2:g.55053183G= GRCh38
NC_000001.10:g.55518856G= , CM000663.1:g.55518856G= GRCh37
NC_000001.9:g.55291444G= NCBI36
NG_009061.1:g.18637G= , LRG_275:g.18637G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.799+392G= ENSP00000501161.2:n.799+392G=
ENST00000710286.1:c.1156+392G= ENSP00000518176.1:n.1156+392G=
ENST00000673903.1:c.424+392G= ENSP00000501257.1:n.424+392G=
ENST00000302118.5:c.799+392G= MANE Select ENSP00000303208.5:n.799+392G=
ENST00000490692.1:n.1620+392G=
NM_174936.3:c.799+392G= , LRG_275t1:c.799+392G= NP_777596.2:n.799+392G=
NR_110451.1:n.458+392G=
NM_174936.4:c.799+392G= MANE Select NP_777596.2:n.799+392G=
NR_110451.2:n.458+392G=
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