Canonical Allele Identifier: CA1167984994
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059753T= , CM000663.2:g.55059753T= GRCh38
NC_000001.10:g.55525426T= , CM000663.1:g.55525426T= GRCh37
NC_000001.9:g.55298014T= NCBI36
NG_009061.1:g.25207T= , LRG_275:g.25207T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1681+90T= ENSP00000501161.2:n.1681+90T=
ENST00000710286.1:c.2038+90T= ENSP00000518176.1:n.2038+90T=
ENST00000673903.1:c.1306+90T= ENSP00000501257.1:n.1306+90T=
ENST00000673913.1:c.421+90T= ENSP00000501161.1:n.421+90T=
ENST00000302118.5:c.1681+90T= MANE Select ENSP00000303208.5:n.1681+90T=
ENST00000490692.1:n.2227+1106T=
NM_174936.3:c.1681+90T= , LRG_275t1:c.1681+90T= NP_777596.2:n.1681+90T=
NR_110451.1:n.1288+90T=
XM_011541193.1:c.802+90T= XP_011539495.1:n.802+90T=
NM_174936.4:c.1681+90T= MANE Select NP_777596.2:n.1681+90T=
NR_110451.2:n.1288+90T=
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