Canonical Allele Identifier: CA1167985026
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059818C= , CM000663.2:g.55059818C= GRCh38
NC_000001.10:g.55525491C= , CM000663.1:g.55525491C= GRCh37
NC_000001.9:g.55298079C= NCBI36
NG_009061.1:g.25272C= , LRG_275:g.25272C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1681+155C= ENSP00000501161.2:n.1681+155C=
ENST00000710286.1:c.2038+155C= ENSP00000518176.1:n.2038+155C=
ENST00000673903.1:c.1306+155C= ENSP00000501257.1:n.1306+155C=
ENST00000673913.1:c.421+155C= ENSP00000501161.1:n.421+155C=
ENST00000302118.5:c.1681+155C= MANE Select ENSP00000303208.5:n.1681+155C=
ENST00000490692.1:n.2227+1171C=
NM_174936.3:c.1681+155C= , LRG_275t1:c.1681+155C= NP_777596.2:n.1681+155C=
NR_110451.1:n.1288+155C=
XM_011541193.1:c.802+155C= XP_011539495.1:n.802+155C=
NM_174936.4:c.1681+155C= MANE Select NP_777596.2:n.1681+155C=
NR_110451.2:n.1288+155C=