Canonical Allele Identifier: CA1167986578
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063613G= , CM000663.2:g.55063613G= GRCh38
NC_000001.10:g.55529286G= , CM000663.1:g.55529286G= GRCh37
NC_000001.9:g.55301874G= NCBI36
NG_009061.1:g.29067G= , LRG_275:g.29067G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*448G= ENSP00000501161.2:n.*448G=
ENST00000710286.1:c.*29G= ENSP00000518176.1:n.*29G=
ENST00000673903.1:c.*29G= ENSP00000501257.1:n.*29G=
ENST00000302118.5:c.*29G= MANE Select ENSP00000303208.5:n.*29G=
ENST00000490692.1:n.2654G=
NM_174936.3:c.*29G= , LRG_275t1:c.*29G= NP_777596.2:n.*29G=
NR_110451.1:n.1715G=
XM_011541193.1:c.*29G= XP_011539495.1:n.*29G=
NM_174936.4:c.*29G= MANE Select NP_777596.2:n.*29G=
NR_110451.2:n.1715G=