Canonical Allele Identifier: CA386015951

Gene: DCN

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91151683C>T , CM000674.2:g.91151683C>T	GRCh38
NC_000012.11:g.91545460C>T , CM000674.1:g.91545460C>T	GRCh37
NC_000012.10:g.90069591C>T	NCBI36
NG_011672.1:g.36347G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000052754.10:c.856G>A MANE Select	ENSP00000052754.5:p.Gly286Ser
ENST00000393155.6:c.*509G>A	ENSP00000376862.2:n.*509G>A
ENST00000052754.9:c.856G>A	ENSP00000052754.5:p.Gly286Ser
ENST00000393155.5:c.856G>A	ENSP00000376862.1:p.Gly286Ser
ENST00000420120.6:c.529G>A	ENSP00000413723.2:p.Gly177Ser
ENST00000425043.5:c.415G>A	ENSP00000401021.1:p.Gly139Ser
ENST00000441303.6:c.325-5431G>A	ENSP00000399815.2:n.325-5431G>A
ENST00000456569.2:c.212-5431G>A	ENSP00000398514.2:n.212-5431G>A
ENST00000546391.5:c.415G>A	ENSP00000446530.1:p.Gly139Ser
ENST00000547568.6:c.415G>A	ENSP00000447674.2:p.Gly139Ser
ENST00000550758.1:c.164G>A
ENST00000552962.5:c.856G>A	ENSP00000447654.1:p.Gly286Ser
NM_001920.3:c.856G>A	NP_001911.1:p.Gly286Ser
NM_001920.4:c.856G>A	NP_001911.1:p.Gly286Ser
NM_133503.2:c.856G>A	NP_598010.1:p.Gly286Ser
NM_133503.3:c.856G>A	NP_598010.1:p.Gly286Ser
NM_133504.2:c.529G>A	NP_598011.1:p.Gly177Ser
NM_133504.3:c.529G>A	NP_598011.1:p.Gly177Ser
NM_133505.2:c.415G>A	NP_598012.1:p.Gly139Ser
NM_133505.3:c.415G>A	NP_598012.1:p.Gly139Ser
NM_133506.2:c.325-5431G>A	NP_598013.1:n.325-5431G>A
NM_133506.3:c.325-5431G>A	NP_598013.1:n.325-5431G>A
NM_133507.2:c.212-5431G>A	NP_598014.1:n.212-5431G>A
NM_133507.3:c.212-5431G>A	NP_598014.1:n.212-5431G>A
XM_005268693.1:c.856G>A	XP_005268750.1:p.Gly286Ser
XM_006719270.1:c.856G>A	XP_006719333.1:p.Gly286Ser
XM_017018917.1:c.856G>A	XP_016874406.1:p.Gly286Ser
NM_001920.5:c.856G>A MANE Select	NP_001911.1:p.Gly286Ser
NM_133503.4:c.856G>A	NP_598010.1:p.Gly286Ser