Canonical Allele Identifier: CA1167978185
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55044070A= , CM000663.2:g.55044070A= GRCh38
NC_000001.10:g.55509743A= , CM000663.1:g.55509743A= GRCh37
NC_000001.9:g.55282331A= NCBI36
NG_009061.1:g.9524A= , LRG_275:g.9524A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.399+36A= ENSP00000501161.2:n.399+36A=
ENST00000710286.1:c.756+36A= ENSP00000518176.1:n.756+36A=
ENST00000673662.1:n.69+36A=
ENST00000673726.1:c.399+36A= ENSP00000501004.1:n.399+36A=
ENST00000673903.1:c.24+36A= ENSP00000501257.1:n.24+36A=
ENST00000302118.5:c.399+36A= MANE Select ENSP00000303208.5:n.399+36A=
NM_174936.3:c.399+36A= , LRG_275t1:c.399+36A= NP_777596.2:n.399+36A=
NR_110451.1:n.182+3667A=
NM_174936.4:c.399+36A= MANE Select NP_777596.2:n.399+36A=
NR_110451.2:n.182+3667A=
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