Canonical Allele Identifier: CA1167984988
Gene: PCSK9 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059728C= , CM000663.2:g.55059728C= GRCh38
NC_000001.10:g.55525401C= , CM000663.1:g.55525401C= GRCh37
NC_000001.9:g.55297989C= NCBI36
NG_009061.1:g.25182C= , LRG_275:g.25182C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1681+65C= ENSP00000501161.2:n.1681+65C=
ENST00000710286.1:c.2038+65C= ENSP00000518176.1:n.2038+65C=
ENST00000673903.1:c.1306+65C= ENSP00000501257.1:n.1306+65C=
ENST00000673913.1:c.421+65C= ENSP00000501161.1:n.421+65C=
ENST00000302118.5:c.1681+65C= MANE Select ENSP00000303208.5:n.1681+65C=
ENST00000490692.1:n.2227+1081C=
NM_174936.3:c.1681+65C= , LRG_275t1:c.1681+65C= NP_777596.2:n.1681+65C=
NR_110451.1:n.1288+65C=
XM_011541193.1:c.802+65C= XP_011539495.1:n.802+65C=
NM_174936.4:c.1681+65C= MANE Select NP_777596.2:n.1681+65C=
NR_110451.2:n.1288+65C=
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