Canonical Allele Identifier: CA341874
Gene: DCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91146199del , CM000674.2:g.91146199del GRCh38
NC_000012.11:g.91539976del , CM000674.1:g.91539976del GRCh37
NC_000012.10:g.90064107del NCBI36
NG_011672.1:g.41833del

Transcript Alleles

HGVS Amino-acid Change
ENST00000052754.10:c.941del MANE Select ENSP00000052754.5:p.Pro314HisfsTer14
ENST00000393155.6:c.*594del ENSP00000376862.2:n.*594del
ENST00000052754.9:c.941del ENSP00000052754.5:p.Pro314HisfsTer14
ENST00000393155.5:c.941del ENSP00000376862.1:p.Pro314HisfsTer14
ENST00000420120.6:c.614del ENSP00000413723.2:p.Pro205HisfsTer14
ENST00000425043.5:c.500del ENSP00000401021.1:p.Pro167HisfsTer14
ENST00000441303.6:c.380del ENSP00000399815.2:p.Pro127HisfsTer14
ENST00000546391.5:c.500del ENSP00000446530.1:p.Pro167HisfsTer?
ENST00000547568.6:c.500del ENSP00000447674.2:p.Pro167HisfsTer14
ENST00000548218.1:c.12del
ENST00000552962.5:c.941del ENSP00000447654.1:p.Pro314HisfsTer14
NM_001920.3:c.941del NP_001911.1:p.Pro314HisfsTer14
NM_001920.4:c.941del NP_001911.1:p.Pro314HisfsTer14
NM_133503.2:c.941del NP_598010.1:p.Pro314HisfsTer14
NM_133503.3:c.941del NP_598010.1:p.Pro314HisfsTer14
NM_133504.2:c.614del NP_598011.1:p.Pro205HisfsTer14
NM_133504.3:c.614del NP_598011.1:p.Pro205HisfsTer14
NM_133505.2:c.500del NP_598012.1:p.Pro167HisfsTer14
NM_133505.3:c.500del NP_598012.1:p.Pro167HisfsTer14
NM_133506.2:c.380del NP_598013.1:p.Pro127HisfsTer14
NM_133506.3:c.380del NP_598013.1:p.Pro127HisfsTer14
NM_133507.2:c.267del NP_598014.1:n.267del
NM_133507.3:c.*39del NP_598014.1:n.*39del
XM_005268693.1:c.941del XP_005268750.1:p.Pro314HisfsTer14
XM_006719270.1:c.941del XP_006719333.1:p.Pro314HisfsTer14
XM_017018917.1:c.941del XP_016874406.1:p.Pro314HisfsTer14
NM_001920.5:c.941del MANE Select NP_001911.1:p.Pro314HisfsTer14
NM_133503.4:c.941del NP_598010.1:p.Pro314HisfsTer14