Canonical Allele Identifier: CA1144140658
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55044038A= , CM000663.2:g.55044038A= GRCh38
NC_000001.10:g.55509711A= , CM000663.1:g.55509711A= GRCh37
NC_000001.9:g.55282299A= NCBI36
NG_009061.1:g.9492A= , LRG_275:g.9492A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.399+4A= ENSP00000501161.2:n.399+4A=
ENST00000710286.1:c.756+4A= ENSP00000518176.1:n.756+4A=
ENST00000673662.1:n.69+4A=
ENST00000673726.1:c.399+4A= ENSP00000501004.1:n.399+4A=
ENST00000673903.1:c.24+4A= ENSP00000501257.1:n.24+4A=
ENST00000302118.5:c.399+4A= MANE Select ENSP00000303208.5:n.399+4A=
NM_174936.3:c.399+4A= , LRG_275t1:c.399+4A= NP_777596.2:n.399+4A=
NR_110451.1:n.182+3635A=
NM_174936.4:c.399+4A= MANE Select NP_777596.2:n.399+4A=
NR_110451.2:n.182+3635A=