Canonical Allele Identifier: CA1167981833
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55053029C= , CM000663.2:g.55053029C= GRCh38
NC_000001.10:g.55518702C= , CM000663.1:g.55518702C= GRCh37
NC_000001.9:g.55291290C= NCBI36
NG_009061.1:g.18483C= , LRG_275:g.18483C=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.799+238C= ENSP00000501161.2:n.799+238C=
ENST00000710286.1:c.1156+238C= ENSP00000518176.1:n.1156+238C=
ENST00000673903.1:c.424+238C= ENSP00000501257.1:n.424+238C=
ENST00000302118.5:c.799+238C= MANE Select ENSP00000303208.5:n.799+238C=
ENST00000490692.1:n.1620+238C=
NM_174936.3:c.799+238C= , LRG_275t1:c.799+238C= NP_777596.2:n.799+238C=
NR_110451.1:n.458+238C=
NM_174936.4:c.799+238C= MANE Select NP_777596.2:n.799+238C=
NR_110451.2:n.458+238C=
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