Canonical Allele Identifier: CA6716901

Gene: DCN

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91146221A>G , CM000674.2:g.91146221A>G	GRCh38
NC_000012.11:g.91539998A>G , CM000674.1:g.91539998A>G	GRCh37
NC_000012.10:g.90064129A>G	NCBI36
NG_011672.1:g.41809T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000052754.10:c.917T>C MANE Select	ENSP00000052754.5:p.Val306Ala
ENST00000393155.6:c.*570T>C	ENSP00000376862.2:n.*570T>C
ENST00000052754.9:c.917T>C	ENSP00000052754.5:p.Val306Ala
ENST00000393155.5:c.917T>C	ENSP00000376862.1:p.Val306Ala
ENST00000420120.6:c.590T>C	ENSP00000413723.2:p.Val197Ala
ENST00000425043.5:c.476T>C	ENSP00000401021.1:p.Val159Ala
ENST00000441303.6:c.356T>C	ENSP00000399815.2:p.Val119Ala
ENST00000546391.5:c.476T>C	ENSP00000446530.1:p.Val159Ala
ENST00000547568.6:c.476T>C	ENSP00000447674.2:p.Val159Ala
ENST00000552962.5:c.917T>C	ENSP00000447654.1:p.Val306Ala
NM_001920.3:c.917T>C	NP_001911.1:p.Val306Ala
NM_001920.4:c.917T>C	NP_001911.1:p.Val306Ala
NM_133503.2:c.917T>C	NP_598010.1:p.Val306Ala
NM_133503.3:c.917T>C	NP_598010.1:p.Val306Ala
NM_133504.2:c.590T>C	NP_598011.1:p.Val197Ala
NM_133504.3:c.590T>C	NP_598011.1:p.Val197Ala
NM_133505.2:c.476T>C	NP_598012.1:p.Val159Ala
NM_133505.3:c.476T>C	NP_598012.1:p.Val159Ala
NM_133506.2:c.356T>C	NP_598013.1:p.Val119Ala
NM_133506.3:c.356T>C	NP_598013.1:p.Val119Ala
NM_133507.2:c.243T>C	NP_598014.1:n.243T>C
NM_133507.3:c.*15T>C	NP_598014.1:n.*15T>C
XM_005268693.1:c.917T>C	XP_005268750.1:p.Val306Ala
XM_006719270.1:c.917T>C	XP_006719333.1:p.Val306Ala
XM_017018917.1:c.917T>C	XP_016874406.1:p.Val306Ala
NM_001920.5:c.917T>C MANE Select	NP_001911.1:p.Val306Ala
NM_133503.4:c.917T>C	NP_598010.1:p.Val306Ala