Canonical Allele Identifier: CA1149061558
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55043870G= , CM000663.2:g.55043870G= GRCh38
NC_000001.10:g.55509543G= , CM000663.1:g.55509543G= GRCh37
NC_000001.9:g.55282131G= NCBI36
NG_009061.1:g.9324G= , LRG_275:g.9324G=

Transcript Alleles

HGVS Amino-acid change
ENST00000673913.2:c.235G= ENSP00000501161.2:p.Val79=
ENST00000710286.1:c.592G= ENSP00000518176.1:p.Val198=
ENST00000673726.1:c.235G= ENSP00000501004.1:p.Val79=
ENST00000673903.1:c.-141G= ENSP00000501257.1:n.-141G=
ENST00000302118.5:c.235G= MANE Select ENSP00000303208.5:p.Val79=
NM_174936.3:c.235G= , LRG_275t1:c.235G= NP_777596.2:p.Val79=
NR_110451.1:n.182+3467G=
NM_174936.4:c.235G= MANE Select NP_777596.2:p.Val79=
NR_110451.2:n.182+3467G=