Canonical Allele Identifier: CA1167978184
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55044069T= , CM000663.2:g.55044069T= GRCh38
NC_000001.10:g.55509742T= , CM000663.1:g.55509742T= GRCh37
NC_000001.9:g.55282330T= NCBI36
NG_009061.1:g.9523T= , LRG_275:g.9523T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.399+35T= ENSP00000501161.2:n.399+35T=
ENST00000710286.1:c.756+35T= ENSP00000518176.1:n.756+35T=
ENST00000673662.1:n.69+35T=
ENST00000673726.1:c.399+35T= ENSP00000501004.1:n.399+35T=
ENST00000673903.1:c.24+35T= ENSP00000501257.1:n.24+35T=
ENST00000302118.5:c.399+35T= MANE Select ENSP00000303208.5:n.399+35T=
NM_174936.3:c.399+35T= , LRG_275t1:c.399+35T= NP_777596.2:n.399+35T=
NR_110451.1:n.182+3666T=
NM_174936.4:c.399+35T= MANE Select NP_777596.2:n.399+35T=
NR_110451.2:n.182+3666T=
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