Canonical Allele Identifier: CA1167986457
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063333C= , CM000663.2:g.55063333C= GRCh38
NC_000001.10:g.55529006C= , CM000663.1:g.55529006C= GRCh37
NC_000001.9:g.55301594C= NCBI36
NG_009061.1:g.28787C= , LRG_275:g.28787C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*204-36C= ENSP00000501161.2:n.*204-36C=
ENST00000710286.1:c.2221-36C= ENSP00000518176.1:n.2221-36C=
ENST00000673903.1:c.1489-36C= ENSP00000501257.1:n.1489-36C=
ENST00000673913.1:c.714-36C= ENSP00000501161.1:n.714-36C=
ENST00000302118.5:c.1864-36C= MANE Select ENSP00000303208.5:n.1864-36C=
ENST00000490692.1:n.2410-36C=
NM_174936.3:c.1864-36C= , LRG_275t1:c.1864-36C= NP_777596.2:n.1864-36C=
NR_110451.1:n.1471-36C=
XM_011541193.1:c.985-36C= XP_011539495.1:n.985-36C=
NM_174936.4:c.1864-36C= MANE Select NP_777596.2:n.1864-36C=
NR_110451.2:n.1471-36C=
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