Canonical Allele Identifier: CA340480299
Gene: PCSK9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061450A>G , CM000663.2:g.55061450A>G GRCh38
NC_000001.10:g.55527123A>G , CM000663.1:g.55527123A>G GRCh37
NC_000001.9:g.55299711A>G NCBI36
NG_009061.1:g.26904A>G , LRG_275:g.26904A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*97A>G ENSP00000501161.2:n.*97A>G
ENST00000710286.1:c.2114A>G ENSP00000518176.1:p.Asn705Ser
ENST00000673903.1:c.1382A>G ENSP00000501257.1:p.Asn461Ser
ENST00000673913.1:c.607A>G ENSP00000501161.1:n.607A>G
ENST00000302118.5:c.1757A>G MANE Select ENSP00000303208.5:p.Asn586Ser
ENST00000490692.1:n.2303A>G
NM_174936.3:c.1757A>G , LRG_275t1:c.1757A>G NP_777596.2:p.Asn586Ser
NR_110451.1:n.1364A>G
XM_011541193.1:c.878A>G XP_011539495.1:p.Asn293Ser
NM_174936.4:c.1757A>G MANE Select NP_777596.2:p.Asn586Ser
NR_110451.2:n.1364A>G