Canonical Allele Identifier: CA1167985028
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059831C= , CM000663.2:g.55059831C= GRCh38
NC_000001.10:g.55525504C= , CM000663.1:g.55525504C= GRCh37
NC_000001.9:g.55298092C= NCBI36
NG_009061.1:g.25285C= , LRG_275:g.25285C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1681+168C= ENSP00000501161.2:n.1681+168C=
ENST00000710286.1:c.2038+168C= ENSP00000518176.1:n.2038+168C=
ENST00000673903.1:c.1306+168C= ENSP00000501257.1:n.1306+168C=
ENST00000673913.1:c.421+168C= ENSP00000501161.1:n.421+168C=
ENST00000302118.5:c.1681+168C= MANE Select ENSP00000303208.5:n.1681+168C=
ENST00000490692.1:n.2227+1184C=
NM_174936.3:c.1681+168C= , LRG_275t1:c.1681+168C= NP_777596.2:n.1681+168C=
NR_110451.1:n.1288+168C=
XM_011541193.1:c.802+168C= XP_011539495.1:n.802+168C=
NM_174936.4:c.1681+168C= MANE Select NP_777596.2:n.1681+168C=
NR_110451.2:n.1288+168C=