Canonical Allele Identifier: CA340480923
Gene: PCSK9 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.55529237G>A (hg19) chr1:g.55063564G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063564G>A , CM000663.2:g.55063564G>A GRCh38
NC_000001.10:g.55529237G>A , CM000663.1:g.55529237G>A GRCh37
NC_000001.9:g.55301825G>A NCBI36
NG_009061.1:g.29018G>A , LRG_275:g.29018G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*399G>A ENSP00000501161.2:n.*399G>A
ENST00000710286.1:c.2416G>A ENSP00000518176.1:p.Ala806Thr
ENST00000673903.1:c.1684G>A ENSP00000501257.1:p.Ala562Thr
ENST00000302118.5:c.2059G>A MANE Select ENSP00000303208.5:p.Ala687Thr
ENST00000490692.1:n.2605G>A
NM_174936.3:c.2059G>A , LRG_275t1:c.2059G>A NP_777596.2:p.Ala687Thr
NR_110451.1:n.1666G>A
XM_011541193.1:c.1180G>A XP_011539495.1:p.Ala394Thr
NM_174936.4:c.2059G>A MANE Select NP_777596.2:p.Ala687Thr
NR_110451.2:n.1666G>A
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