Canonical Allele Identifier: CA1167984991
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059742C= , CM000663.2:g.55059742C= GRCh38
NC_000001.10:g.55525415C= , CM000663.1:g.55525415C= GRCh37
NC_000001.9:g.55298003C= NCBI36
NG_009061.1:g.25196C= , LRG_275:g.25196C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1681+79C= ENSP00000501161.2:n.1681+79C=
ENST00000710286.1:c.2038+79C= ENSP00000518176.1:n.2038+79C=
ENST00000673903.1:c.1306+79C= ENSP00000501257.1:n.1306+79C=
ENST00000673913.1:c.421+79C= ENSP00000501161.1:n.421+79C=
ENST00000302118.5:c.1681+79C= MANE Select ENSP00000303208.5:n.1681+79C=
ENST00000490692.1:n.2227+1095C=
NM_174936.3:c.1681+79C= , LRG_275t1:c.1681+79C= NP_777596.2:n.1681+79C=
NR_110451.1:n.1288+79C=
XM_011541193.1:c.802+79C= XP_011539495.1:n.802+79C=
NM_174936.4:c.1681+79C= MANE Select NP_777596.2:n.1681+79C=
NR_110451.2:n.1288+79C=