Canonical Allele Identifier: CA1655198636

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061098C= , CM000668.2:g.112061098C=	GRCh38
NC_000006.11:g.112382301C= , CM000668.1:g.112382301C=	GRCh37
NC_000006.10:g.112488994C=	NCBI36
NG_011748.1:g.12024C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.156C= MANE Select	ENSP00000357655.4:p.Cys52=
ENST00000639360.1:c.60C=	ENSP00000491774.1:p.Cys20=
ENST00000230529.9:c.156C=	ENSP00000230529.5:p.Cys52=
ENST00000361714.5:c.156C=	ENSP00000354734.2:p.Cys52=
ENST00000368663.4:c.156C=	ENSP00000357652.4:p.Cys52=
ENST00000368664.7:c.210C=	ENSP00000357653.3:p.Cys70=
ENST00000368666.6:c.210C=	ENSP00000357655.3:p.Cys70=
ENST00000409166.5:c.-507-181C=	ENSP00000386467.1:n.-507-181C=
ENST00000454589.5:c.156C=	ENSP00000395928.1:p.Cys52=
ENST00000604763.5:c.156C=	ENSP00000473777.1:p.Cys52=
ENST00000620524.3:n.90C=
NM_003880.3:c.156C=	NP_003871.1:p.Cys52=
NM_198239.1:c.210C=	NP_937882.1:p.Cys70=
NR_125353.1:n.346C=
NR_125354.1:n.266C=
XM_011536220.1:c.156C=	XP_011534522.1:p.Cys52=
XM_011536221.1:c.219C=	XP_011534523.1:p.Cys73=
XM_011536222.1:c.294C=	XP_011534524.1:p.Cys98=
XM_011536222.2:c.219C=	XP_011534524.2:p.Cys73=
XR_001743705.1:n.694C=
NM_003880.4:c.156C=	NP_003871.1:p.Cys52=
NM_198239.2:c.156C= MANE Select	NP_937882.2:p.Cys52=
NR_125353.2:n.410C=
NR_125354.3:n.237C=