Canonical Allele Identifier: CA2054337779
Gene: DCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91163515T>G , CM000674.2:g.91163515T>G GRCh38
NC_000012.11:g.91557292T>G , CM000674.1:g.91557292T>G GRCh37
NC_000012.10:g.90081423T>G NCBI36
NG_011672.1:g.24515A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000052754.10:c.324+1090A>C MANE Select ENSP00000052754.5:n.324+1090A>C
ENST00000393155.6:c.212-5006A>C ENSP00000376862.2:n.212-5006A>C
ENST00000052754.9:c.324+1090A>C ENSP00000052754.5:n.324+1090A>C
ENST00000393155.5:c.324+1090A>C ENSP00000376862.1:n.324+1090A>C
ENST00000420120.6:c.212-6327A>C ENSP00000413723.2:n.212-6327A>C
ENST00000425043.5:c.212-10326A>C ENSP00000401021.1:n.212-10326A>C
ENST00000441303.6:c.324+1090A>C ENSP00000399815.2:n.324+1090A>C
ENST00000456569.2:c.211+14827A>C ENSP00000398514.2:n.211+14827A>C
ENST00000546391.5:c.212-10326A>C ENSP00000446530.1:n.212-10326A>C
ENST00000547568.6:c.212-10326A>C ENSP00000447674.2:n.212-10326A>C
ENST00000547937.5:c.324+1090A>C ENSP00000449782.1:n.324+1090A>C
ENST00000549513.5:c.324+1090A>C ENSP00000449438.1:n.324+1090A>C
ENST00000550563.5:c.324+1090A>C ENSP00000449014.1:n.324+1090A>C
ENST00000552145.5:c.324+1090A>C ENSP00000447886.1:n.324+1090A>C
ENST00000552962.5:c.324+1090A>C ENSP00000447654.1:n.324+1090A>C
NM_001920.3:c.324+1090A>C NP_001911.1:n.324+1090A>C
NM_001920.4:c.324+1090A>C NP_001911.1:n.324+1090A>C
NM_133503.2:c.324+1090A>C NP_598010.1:n.324+1090A>C
NM_133503.3:c.324+1090A>C NP_598010.1:n.324+1090A>C
NM_133504.2:c.212-6327A>C NP_598011.1:n.212-6327A>C
NM_133504.3:c.212-6327A>C NP_598011.1:n.212-6327A>C
NM_133505.2:c.212-10326A>C NP_598012.1:n.212-10326A>C
NM_133505.3:c.212-10326A>C NP_598012.1:n.212-10326A>C
NM_133506.2:c.324+1090A>C NP_598013.1:n.324+1090A>C
NM_133506.3:c.324+1090A>C NP_598013.1:n.324+1090A>C
NM_133507.2:c.211+14827A>C NP_598014.1:n.211+14827A>C
NM_133507.3:c.211+14827A>C NP_598014.1:n.211+14827A>C
XM_005268693.1:c.324+1090A>C XP_005268750.1:n.324+1090A>C
XM_006719270.1:c.324+1090A>C XP_006719333.1:n.324+1090A>C
XM_017018917.1:c.324+1090A>C XP_016874406.1:n.324+1090A>C
NM_001920.5:c.324+1090A>C MANE Select NP_001911.1:n.324+1090A>C
NM_133503.4:c.324+1090A>C NP_598010.1:n.324+1090A>C