Canonical Allele Identifier: CA6717111

Gene: DCN

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91164647G>A , CM000674.2:g.91164647G>A	GRCh38
NC_000012.11:g.91558424G>A , CM000674.1:g.91558424G>A	GRCh37
NC_000012.10:g.90082555G>A	NCBI36
NG_011672.1:g.23383C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000052754.10:c.282C>T MANE Select	ENSP00000052754.5:p.Thr94=
ENST00000393155.6:c.212-6138C>T	ENSP00000376862.2:n.212-6138C>T
ENST00000052754.9:c.282C>T	ENSP00000052754.5:p.Thr94=
ENST00000393155.5:c.282C>T	ENSP00000376862.1:p.Thr94=
ENST00000420120.6:c.212-7459C>T	ENSP00000413723.2:n.212-7459C>T
ENST00000425043.5:c.212-11458C>T	ENSP00000401021.1:n.212-11458C>T
ENST00000441303.6:c.282C>T	ENSP00000399815.2:p.Thr94=
ENST00000456569.2:c.211+13695C>T	ENSP00000398514.2:n.211+13695C>T
ENST00000546391.5:c.212-11458C>T	ENSP00000446530.1:n.212-11458C>T
ENST00000547568.6:c.212-11458C>T	ENSP00000447674.2:n.212-11458C>T
ENST00000547937.5:c.282C>T	ENSP00000449782.1:p.Thr94=
ENST00000549513.5:c.282C>T	ENSP00000449438.1:p.Thr94=
ENST00000550563.5:c.282C>T	ENSP00000449014.1:p.Thr94=
ENST00000552145.5:c.282C>T	ENSP00000447886.1:p.Thr94=
ENST00000552962.5:c.282C>T	ENSP00000447654.1:p.Thr94=
NM_001920.3:c.282C>T	NP_001911.1:p.Thr94=
NM_001920.4:c.282C>T	NP_001911.1:p.Thr94=
NM_133503.2:c.282C>T	NP_598010.1:p.Thr94=
NM_133503.3:c.282C>T	NP_598010.1:p.Thr94=
NM_133504.2:c.212-7459C>T	NP_598011.1:n.212-7459C>T
NM_133504.3:c.212-7459C>T	NP_598011.1:n.212-7459C>T
NM_133505.2:c.212-11458C>T	NP_598012.1:n.212-11458C>T
NM_133505.3:c.212-11458C>T	NP_598012.1:n.212-11458C>T
NM_133506.2:c.282C>T	NP_598013.1:p.Thr94=
NM_133506.3:c.282C>T	NP_598013.1:p.Thr94=
NM_133507.2:c.211+13695C>T	NP_598014.1:n.211+13695C>T
NM_133507.3:c.211+13695C>T	NP_598014.1:n.211+13695C>T
XM_005268693.1:c.282C>T	XP_005268750.1:p.Thr94=
XM_006719270.1:c.282C>T	XP_006719333.1:p.Thr94=
XM_017018917.1:c.282C>T	XP_016874406.1:p.Thr94=
NM_001920.5:c.282C>T MANE Select	NP_001911.1:p.Thr94=
NM_133503.4:c.282C>T	NP_598010.1:p.Thr94=