Canonical Allele Identifier: CA10643511

Gene: DCN

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91145769T>A , CM000674.2:g.91145769T>A	GRCh38
NC_000012.11:g.91539546T>A , CM000674.1:g.91539546T>A	GRCh37
NC_000012.10:g.90063677T>A	NCBI36
NG_011672.1:g.42261A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000052754.10:c.*289A>T MANE Select	ENSP00000052754.5:n.*289A>T
ENST00000393155.6:c.*1022A>T	ENSP00000376862.2:n.*1022A>T
ENST00000052754.9:c.*289A>T	ENSP00000052754.5:n.*289A>T
ENST00000393155.5:c.*289A>T	ENSP00000376862.1:n.*289A>T
ENST00000425043.5:c.928A>T	ENSP00000401021.1:n.928A>T
ENST00000548218.1:c.148-35A>T
ENST00000552962.5:c.*289A>T	ENSP00000447654.1:n.*289A>T
NM_001920.3:c.*289A>T	NP_001911.1:n.*289A>T
NM_001920.4:c.*289A>T	NP_001911.1:n.*289A>T
NM_133503.2:c.*289A>T	NP_598010.1:n.*289A>T
NM_133503.3:c.*289A>T	NP_598010.1:n.*289A>T
NM_133504.2:c.1042A>T	NP_598011.1:n.1042A>T
NM_133504.3:c.*289A>T	NP_598011.1:n.*289A>T
NM_133505.2:c.928A>T	NP_598012.1:n.928A>T
NM_133505.3:c.*289A>T	NP_598012.1:n.*289A>T
NM_133506.2:c.808A>T	NP_598013.1:n.808A>T
NM_133506.3:c.*289A>T	NP_598013.1:n.*289A>T
NM_133507.2:c.695A>T	NP_598014.1:n.695A>T
NM_133507.3:c.*467A>T	NP_598014.1:n.*467A>T
XM_005268693.1:c.*289A>T	XP_005268750.1:n.*289A>T
XM_006719270.1:c.*289A>T	XP_006719333.1:n.*289A>T
XM_017018917.1:c.*289A>T	XP_016874406.1:n.*289A>T
NM_001920.5:c.*289A>T MANE Select	NP_001911.1:n.*289A>T
NM_133503.4:c.*289A>T	NP_598010.1:n.*289A>T