Canonical Allele Identifier: CA340480444
Gene: PCSK9 HGNC NCBI

Linked Data

gnomAD v4: 1-55061516-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061516G>A , CM000663.2:g.55061516G>A GRCh38
NC_000001.10:g.55527189G>A , CM000663.1:g.55527189G>A GRCh37
NC_000001.9:g.55299777G>A NCBI36
NG_009061.1:g.26970G>A , LRG_275:g.26970G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*163G>A ENSP00000501161.2:n.*163G>A
ENST00000710286.1:c.2180G>A ENSP00000518176.1:p.Cys727Tyr
ENST00000673903.1:c.1448G>A ENSP00000501257.1:p.Cys483Tyr
ENST00000673913.1:c.673G>A ENSP00000501161.1:n.673G>A
ENST00000302118.5:c.1823G>A MANE Select ENSP00000303208.5:p.Cys608Tyr
ENST00000490692.1:n.2369G>A
NM_174936.3:c.1823G>A , LRG_275t1:c.1823G>A NP_777596.2:p.Cys608Tyr
NR_110451.1:n.1430G>A
XM_011541193.1:c.944G>A XP_011539495.1:p.Cys315Tyr
NM_174936.4:c.1823G>A MANE Select NP_777596.2:p.Cys608Tyr
NR_110451.2:n.1430G>A