Canonical Allele Identifier: CA340479824
Gene: PCSK9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059541T>G , CM000663.2:g.55059541T>G GRCh38
NC_000001.10:g.55525214T>G , CM000663.1:g.55525214T>G GRCh37
NC_000001.9:g.55297802T>G NCBI36
NG_009061.1:g.24995T>G , LRG_275:g.24995T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1559T>G ENSP00000501161.2:p.Val520Gly
ENST00000710286.1:c.1916T>G ENSP00000518176.1:p.Val639Gly
ENST00000673903.1:c.1184T>G ENSP00000501257.1:p.Val395Gly
ENST00000673913.1:c.299T>G ENSP00000501161.1:p.Val100Gly
ENST00000302118.5:c.1559T>G MANE Select ENSP00000303208.5:p.Val520Gly
ENST00000490692.1:n.2227+894T>G
NM_174936.3:c.1559T>G , LRG_275t1:c.1559T>G NP_777596.2:p.Val520Gly
NR_110451.1:n.1166T>G
XM_011541193.1:c.680T>G XP_011539495.1:p.Val227Gly
NM_174936.4:c.1559T>G MANE Select NP_777596.2:p.Val520Gly
NR_110451.2:n.1166T>G