Canonical Allele Identifier: CA6716854

Gene: DCN

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91145681A>G , CM000674.2:g.91145681A>G	GRCh38
NC_000012.11:g.91539458A>G , CM000674.1:g.91539458A>G	GRCh37
NC_000012.10:g.90063589A>G	NCBI36
NG_011672.1:g.42349T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000052754.10:c.*377T>C MANE Select	ENSP00000052754.5:n.*377T>C
ENST00000393155.6:c.*1110T>C	ENSP00000376862.2:n.*1110T>C
ENST00000052754.9:c.*377T>C	ENSP00000052754.5:n.*377T>C
ENST00000393155.5:c.*377T>C	ENSP00000376862.1:n.*377T>C
ENST00000425043.5:c.1016T>C	ENSP00000401021.1:n.1016T>C
ENST00000548218.1:c.201T>C
NM_001920.3:c.*377T>C	NP_001911.1:n.*377T>C
NM_001920.4:c.*377T>C	NP_001911.1:n.*377T>C
NM_133503.2:c.*377T>C	NP_598010.1:n.*377T>C
NM_133503.3:c.*377T>C	NP_598010.1:n.*377T>C
NM_133504.2:c.1130T>C	NP_598011.1:n.1130T>C
NM_133504.3:c.*377T>C	NP_598011.1:n.*377T>C
NM_133505.2:c.1016T>C	NP_598012.1:n.1016T>C
NM_133505.3:c.*377T>C	NP_598012.1:n.*377T>C
NM_133506.2:c.896T>C	NP_598013.1:n.896T>C
NM_133506.3:c.*377T>C	NP_598013.1:n.*377T>C
NM_133507.2:c.783T>C	NP_598014.1:n.783T>C
NM_133507.3:c.*555T>C	NP_598014.1:n.*555T>C
XM_005268693.1:c.*377T>C	XP_005268750.1:n.*377T>C
XM_006719270.1:c.*377T>C	XP_006719333.1:n.*377T>C
XM_017018917.1:c.*377T>C	XP_016874406.1:n.*377T>C
NM_001920.5:c.*377T>C MANE Select	NP_001911.1:n.*377T>C
NM_133503.4:c.*377T>C	NP_598010.1:n.*377T>C