Canonical Allele Identifier: CA1148117849
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55053111C= , CM000663.2:g.55053111C= GRCh38
NC_000001.10:g.55518784C= , CM000663.1:g.55518784C= GRCh37
NC_000001.9:g.55291372C= NCBI36
NG_009061.1:g.18565C= , LRG_275:g.18565C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.799+320C= ENSP00000501161.2:n.799+320C=
ENST00000710286.1:c.1156+320C= ENSP00000518176.1:n.1156+320C=
ENST00000673903.1:c.424+320C= ENSP00000501257.1:n.424+320C=
ENST00000302118.5:c.799+320C= MANE Select ENSP00000303208.5:n.799+320C=
ENST00000490692.1:n.1620+320C=
NM_174936.3:c.799+320C= , LRG_275t1:c.799+320C= NP_777596.2:n.799+320C=
NR_110451.1:n.458+320C=
NM_174936.4:c.799+320C= MANE Select NP_777596.2:n.799+320C=
NR_110451.2:n.458+320C=