Canonical Allele Identifier: CA365371573

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112064841T>A , CM000668.2:g.112064841T>A	GRCh38
NC_000006.11:g.112386044T>A , CM000668.1:g.112386044T>A	GRCh37
NC_000006.10:g.112492737T>A	NCBI36
NG_011748.1:g.15767T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.433T>A MANE Select	ENSP00000357655.4:p.Cys145Ser
ENST00000639360.1:c.334T>A	ENSP00000491774.1:p.Cys112Ser
ENST00000230529.9:c.433T>A	ENSP00000230529.5:p.Cys145Ser
ENST00000361714.5:c.433T>A	ENSP00000354734.2:p.Cys145Ser
ENST00000368663.4:c.433T>A	ENSP00000357652.4:p.Cys145Ser
ENST00000368664.7:c.487T>A	ENSP00000357653.3:p.Cys163Ser
ENST00000368666.6:c.487T>A	ENSP00000357655.3:p.Cys163Ser
ENST00000409166.5:c.-304T>A	ENSP00000386467.1:n.-304T>A
ENST00000454589.5:c.433T>A	ENSP00000395928.1:p.Cys145Ser
ENST00000604763.5:c.433T>A	ENSP00000473777.1:p.Cys145Ser
ENST00000613648.1:n.204T>A
ENST00000620524.3:n.364T>A
NM_003880.3:c.433T>A	NP_003871.1:p.Cys145Ser
NM_198239.1:c.487T>A	NP_937882.1:p.Cys163Ser
NR_125353.1:n.623T>A
NR_125354.1:n.543T>A
XM_011536220.1:c.433T>A	XP_011534522.1:p.Cys145Ser
XM_011536221.1:c.496T>A	XP_011534523.1:p.Cys166Ser
XM_011536222.1:c.516+55T>A	XP_011534524.1:n.516+55T>A
XM_011536223.1:c.-150T>A	XP_011534525.1:n.-150T>A
XM_011536222.2:c.441+55T>A	XP_011534524.2:n.441+55T>A
XM_011536223.3:c.-150T>A	XP_011534525.1:n.-150T>A
XR_001743705.1:n.971T>A
NM_003880.4:c.433T>A	NP_003871.1:p.Cys145Ser
NM_198239.2:c.433T>A MANE Select	NP_937882.2:p.Cys145Ser
NR_125353.2:n.687T>A
NR_125354.3:n.514T>A