Canonical Allele Identifier: CA341433
Gene: DCN HGNC NCBI

Linked Data

ClinVar Variation Id: 16870
ClinVar RCV Id: RCV000018366
dbSNP Id: rs80338741

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91146172del , CM000674.2:g.91146172del GRCh38
NC_000012.11:g.91539949del , CM000674.1:g.91539949del GRCh37
NC_000012.10:g.90064080del NCBI36
NG_011672.1:g.41859del

Transcript Alleles

HGVS Amino-acid change
ENST00000052754.10:c.967del MANE Select ENSP00000052754.5:p.Ser323LeufsTer5
ENST00000393155.6:c.*620del ENSP00000376862.2:n.*620del
ENST00000052754.9:c.967del ENSP00000052754.5:p.Ser323LeufsTer5
ENST00000393155.5:c.967del ENSP00000376862.1:p.Ser323LeufsTer5
ENST00000420120.6:c.640del ENSP00000413723.2:p.Ser214LeufsTer5
ENST00000425043.5:c.526del ENSP00000401021.1:p.Ser176LeufsTer5
ENST00000441303.6:c.406del ENSP00000399815.2:p.Ser136LeufsTer5
ENST00000546391.5:c.526del ENSP00000446530.1:p.Ser176LeufsTer?
ENST00000547568.6:c.526del ENSP00000447674.2:p.Ser176LeufsTer5
ENST00000548218.1:c.38del
ENST00000552962.5:c.967del ENSP00000447654.1:p.Ser323LeufsTer5
NM_001920.3:c.967del NP_001911.1:p.Ser323LeufsTer5
NM_001920.4:c.967del NP_001911.1:p.Ser323LeufsTer5
NM_133503.2:c.967del NP_598010.1:p.Ser323LeufsTer5
NM_133503.3:c.967del NP_598010.1:p.Ser323LeufsTer5
NM_133504.2:c.640del NP_598011.1:p.Ser214LeufsTer5
NM_133504.3:c.640del NP_598011.1:p.Ser214LeufsTer5
NM_133505.2:c.526del NP_598012.1:p.Ser176LeufsTer5
NM_133505.3:c.526del NP_598012.1:p.Ser176LeufsTer5
NM_133506.2:c.406del NP_598013.1:p.Ser136LeufsTer5
NM_133506.3:c.406del NP_598013.1:p.Ser136LeufsTer5
NM_133507.2:c.293del NP_598014.1:n.293del
NM_133507.3:c.*65del NP_598014.1:n.*65del
XM_005268693.1:c.967del XP_005268750.1:p.Ser323LeufsTer5
XM_006719270.1:c.967del XP_006719333.1:p.Ser323LeufsTer5
XM_017018917.1:c.967del XP_016874406.1:p.Ser323LeufsTer5
NM_001920.5:c.967del MANE Select NP_001911.1:p.Ser323LeufsTer5
NM_133503.4:c.967del NP_598010.1:p.Ser323LeufsTer5