Canonical Allele Identifier: CA6716898

Gene: DCN

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91146194G>T , CM000674.2:g.91146194G>T	GRCh38
NC_000012.11:g.91539971G>T , CM000674.1:g.91539971G>T	GRCh37
NC_000012.10:g.90064102G>T	NCBI36
NG_011672.1:g.41836C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000052754.10:c.944C>A MANE Select	ENSP00000052754.5:p.Pro315His
ENST00000393155.6:c.*597C>A	ENSP00000376862.2:n.*597C>A
ENST00000052754.9:c.944C>A	ENSP00000052754.5:p.Pro315His
ENST00000393155.5:c.944C>A	ENSP00000376862.1:p.Pro315His
ENST00000420120.6:c.617C>A	ENSP00000413723.2:p.Pro206His
ENST00000425043.5:c.503C>A	ENSP00000401021.1:p.Pro168His
ENST00000441303.6:c.383C>A	ENSP00000399815.2:p.Pro128His
ENST00000546391.5:c.503C>A	ENSP00000446530.1:p.Pro168His
ENST00000547568.6:c.503C>A	ENSP00000447674.2:p.Pro168His
ENST00000548218.1:c.15C>A
ENST00000552962.5:c.944C>A	ENSP00000447654.1:p.Pro315His
NM_001920.3:c.944C>A	NP_001911.1:p.Pro315His
NM_001920.4:c.944C>A	NP_001911.1:p.Pro315His
NM_133503.2:c.944C>A	NP_598010.1:p.Pro315His
NM_133503.3:c.944C>A	NP_598010.1:p.Pro315His
NM_133504.2:c.617C>A	NP_598011.1:p.Pro206His
NM_133504.3:c.617C>A	NP_598011.1:p.Pro206His
NM_133505.2:c.503C>A	NP_598012.1:p.Pro168His
NM_133505.3:c.503C>A	NP_598012.1:p.Pro168His
NM_133506.2:c.383C>A	NP_598013.1:p.Pro128His
NM_133506.3:c.383C>A	NP_598013.1:p.Pro128His
NM_133507.2:c.270C>A	NP_598014.1:n.270C>A
NM_133507.3:c.*42C>A	NP_598014.1:n.*42C>A
XM_005268693.1:c.944C>A	XP_005268750.1:p.Pro315His
XM_006719270.1:c.944C>A	XP_006719333.1:p.Pro315His
XM_017018917.1:c.944C>A	XP_016874406.1:p.Pro315His
NM_001920.5:c.944C>A MANE Select	NP_001911.1:p.Pro315His
NM_133503.4:c.944C>A	NP_598010.1:p.Pro315His