Canonical Allele Identifier: CA1167986658
Gene: PCSK9 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.55063789_55063790delinsAG , CM000663.2:g.55063789_55063790delinsAG GRCh38
NC_000001.10:g.55529462_55529463delinsAG , CM000663.1:g.55529462_55529463delinsAG GRCh37
NC_000001.9:g.55302050_55302051delinsAG NCBI36
NG_009061.1:g.29243_29244delinsAG , LRG_275:g.29243_29244delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000673913.2:c.*624_*625delinsAG ENSP00000501161.2:n.*624_*625delinsAG
ENST00000710286.1:c.*205_*206delinsAG ENSP00000518176.1:n.*205_*206delinsAG
ENST00000673903.1:c.*205_*206delinsAG ENSP00000501257.1:n.*205_*206delinsAG
ENST00000302118.5:c.*205_*206delinsAG MANE Select ENSP00000303208.5:n.*205_*206delinsAG
ENST00000490692.1:n.2830_2831delinsAG
NM_174936.3:c.*205_*206delinsAG , LRG_275t1:c.*205_*206delinsAG NP_777596.2:n.*205_*206delinsAG
NR_110451.1:n.1891_1892delinsAG
XM_011541193.1:c.*205_*206delinsAG XP_011539495.1:n.*205_*206delinsAG
NM_174936.4:c.*205_*206delinsAG MANE Select NP_777596.2:n.*205_*206delinsAG
NR_110451.2:n.1891_1892delinsAG