Canonical Allele Identifier: CA1655201603

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069579A= , CM000668.2:g.112069579A=	GRCh38
NC_000006.11:g.112390782A= , CM000668.1:g.112390782A=	GRCh37
NC_000006.10:g.112497475A=	NCBI36
NG_011748.1:g.20505A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1024A= MANE Select	ENSP00000357655.4:p.Arg342=
ENST00000639360.1:c.925A=	ENSP00000491774.1:p.Arg309=
ENST00000230529.9:c.1024A=	ENSP00000230529.5:p.Arg342=
ENST00000361714.5:c.1024A=	ENSP00000354734.2:p.Arg342=
ENST00000368663.4:c.*330A=	ENSP00000357652.4:n.*330A=
ENST00000368664.7:c.*428A=	ENSP00000357653.3:n.*428A=
ENST00000368666.6:c.1078A=	ENSP00000357655.3:p.Arg360=
ENST00000409166.5:c.352A=	ENSP00000386467.1:p.Arg118=
ENST00000454589.5:c.*428A=	ENSP00000395928.1:n.*428A=
ENST00000604763.5:c.1024A=	ENSP00000473777.1:p.Arg342=
ENST00000613648.1:n.859A=
ENST00000620524.3:n.955A=
NM_003880.3:c.1024A=	NP_003871.1:p.Arg342=
NM_198239.1:c.1078A=	NP_937882.1:p.Arg360=
NR_125353.1:n.1278A=
NR_125354.1:n.1198A=
XM_011536220.1:c.1024A=	XP_011534522.1:p.Arg342=
XM_011536221.1:c.*428A=	XP_011534523.1:n.*428A=
XM_011536223.1:c.442A=	XP_011534525.1:p.Arg148=
XM_011536223.3:c.442A=	XP_011534525.1:p.Arg148=
XR_001743705.1:n.1626A=
NM_003880.4:c.1024A=	NP_003871.1:p.Arg342=
NM_198239.2:c.1024A= MANE Select	NP_937882.2:p.Arg342=
NR_125353.2:n.1342A=
NR_125354.3:n.1169A=