Canonical Allele Identifier: CA2645842948
Gene: PCSK9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55061670del , CM000663.2:g.55061670del GRCh38
NC_000001.10:g.55527343del , CM000663.1:g.55527343del GRCh37
NC_000001.9:g.55299931del NCBI36
NG_009061.1:g.27124del , LRG_275:g.27124del

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*203+114del ENSP00000501161.2:n.*203+114del
ENST00000710286.1:c.2220+114del ENSP00000518176.1:n.2220+114del
ENST00000673903.1:c.1488+114del ENSP00000501257.1:n.1488+114del
ENST00000673913.1:c.713+114del ENSP00000501161.1:n.713+114del
ENST00000302118.5:c.1863+114del MANE Select ENSP00000303208.5:n.1863+114del
ENST00000490692.1:n.2409+114del
NM_174936.3:c.1863+114del , LRG_275t1:c.1863+114del NP_777596.2:n.1863+114del
NR_110451.1:n.1470+114del
XM_011541193.1:c.984+114del XP_011539495.1:n.984+114del
NM_174936.4:c.1863+114del MANE Select NP_777596.2:n.1863+114del
NR_110451.2:n.1470+114del