Canonical Allele Identifier: CA2645841808
Gene: PCSK9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55059799del , CM000663.2:g.55059799del GRCh38
NC_000001.10:g.55525472del , CM000663.1:g.55525472del GRCh37
NC_000001.9:g.55298060del NCBI36
NG_009061.1:g.25253del , LRG_275:g.25253del

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.1681+136del ENSP00000501161.2:n.1681+136del
ENST00000710286.1:c.2038+136del ENSP00000518176.1:n.2038+136del
ENST00000673903.1:c.1306+136del ENSP00000501257.1:n.1306+136del
ENST00000673913.1:c.421+136del ENSP00000501161.1:n.421+136del
ENST00000302118.5:c.1681+136del MANE Select ENSP00000303208.5:n.1681+136del
ENST00000490692.1:n.2227+1152del
NM_174936.3:c.1681+136del , LRG_275t1:c.1681+136del NP_777596.2:n.1681+136del
NR_110451.1:n.1288+136del
XM_011541193.1:c.802+136del XP_011539495.1:n.802+136del
NM_174936.4:c.1681+136del MANE Select NP_777596.2:n.1681+136del
NR_110451.2:n.1288+136del