Canonical Allele Identifier: CA6717010

Gene: DCN

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91157106A>C , CM000674.2:g.91157106A>C	GRCh38
NC_000012.11:g.91550883A>C , CM000674.1:g.91550883A>C	GRCh37
NC_000012.10:g.90075014A>C	NCBI36
NG_011672.1:g.30924T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000052754.10:c.621T>G MANE Select	ENSP00000052754.5:p.Ile207Met
ENST00000393155.6:c.*274T>G	ENSP00000376862.2:n.*274T>G
ENST00000052754.9:c.621T>G	ENSP00000052754.5:p.Ile207Met
ENST00000393155.5:c.621T>G	ENSP00000376862.1:p.Ile207Met
ENST00000420120.6:c.294T>G	ENSP00000413723.2:p.Ile98Met
ENST00000425043.5:c.212-3917T>G	ENSP00000401021.1:n.212-3917T>G
ENST00000441303.6:c.324+7499T>G	ENSP00000399815.2:n.324+7499T>G
ENST00000456569.2:c.212-10854T>G	ENSP00000398514.2:n.212-10854T>G
ENST00000546391.5:c.212-3917T>G	ENSP00000446530.1:n.212-3917T>G
ENST00000547568.6:c.212-3917T>G	ENSP00000447674.2:n.212-3917T>G
ENST00000552962.5:c.621T>G	ENSP00000447654.1:p.Ile207Met
NM_001920.3:c.621T>G	NP_001911.1:p.Ile207Met
NM_001920.4:c.621T>G	NP_001911.1:p.Ile207Met
NM_133503.2:c.621T>G	NP_598010.1:p.Ile207Met
NM_133503.3:c.621T>G	NP_598010.1:p.Ile207Met
NM_133504.2:c.294T>G	NP_598011.1:p.Ile98Met
NM_133504.3:c.294T>G	NP_598011.1:p.Ile98Met
NM_133505.2:c.212-3917T>G	NP_598012.1:n.212-3917T>G
NM_133505.3:c.212-3917T>G	NP_598012.1:n.212-3917T>G
NM_133506.2:c.324+7499T>G	NP_598013.1:n.324+7499T>G
NM_133506.3:c.324+7499T>G	NP_598013.1:n.324+7499T>G
NM_133507.2:c.212-10854T>G	NP_598014.1:n.212-10854T>G
NM_133507.3:c.212-10854T>G	NP_598014.1:n.212-10854T>G
XM_005268693.1:c.621T>G	XP_005268750.1:p.Ile207Met
XM_006719270.1:c.621T>G	XP_006719333.1:p.Ile207Met
XM_017018917.1:c.621T>G	XP_016874406.1:p.Ile207Met
NM_001920.5:c.621T>G MANE Select	NP_001911.1:p.Ile207Met
NM_133503.4:c.621T>G	NP_598010.1:p.Ile207Met