Canonical Allele Identifier: CA1167978028
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55043687A= , CM000663.2:g.55043687A= GRCh38
NC_000001.10:g.55509360A= , CM000663.1:g.55509360A= GRCh37
NC_000001.9:g.55281948A= NCBI36
NG_009061.1:g.9141A= , LRG_275:g.9141A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.208-156A= ENSP00000501161.2:n.208-156A=
ENST00000710286.1:c.565-156A= ENSP00000518176.1:n.565-156A=
ENST00000673726.1:c.208-156A= ENSP00000501004.1:n.208-156A=
ENST00000673903.1:c.-168-156A= ENSP00000501257.1:n.-168-156A=
ENST00000302118.5:c.208-156A= MANE Select ENSP00000303208.5:n.208-156A=
NM_174936.3:c.208-156A= , LRG_275t1:c.208-156A= NP_777596.2:n.208-156A=
NR_110451.1:n.182+3284A=
NM_174936.4:c.208-156A= MANE Select NP_777596.2:n.208-156A=
NR_110451.2:n.182+3284A=