Canonical Allele Identifier: CA340479957
Gene: PCSK9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059584C>G , CM000663.2:g.55059584C>G GRCh38
NC_000001.10:g.55525257C>G , CM000663.1:g.55525257C>G GRCh37
NC_000001.9:g.55297845C>G NCBI36
NG_009061.1:g.25038C>G , LRG_275:g.25038C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1602C>G ENSP00000501161.2:p.Cys534Trp
ENST00000710286.1:c.1959C>G ENSP00000518176.1:p.Cys653Trp
ENST00000673903.1:c.1227C>G ENSP00000501257.1:p.Cys409Trp
ENST00000673913.1:c.342C>G ENSP00000501161.1:p.Cys114Trp
ENST00000302118.5:c.1602C>G MANE Select ENSP00000303208.5:p.Cys534Trp
ENST00000490692.1:n.2227+937C>G
NM_174936.3:c.1602C>G , LRG_275t1:c.1602C>G NP_777596.2:p.Cys534Trp
NR_110451.1:n.1209C>G
XM_011541193.1:c.723C>G XP_011539495.1:p.Cys241Trp
NM_174936.4:c.1602C>G MANE Select NP_777596.2:p.Cys534Trp
NR_110451.2:n.1209C>G