Canonical Allele Identifier: CA1655201609

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069595T= , CM000668.2:g.112069595T=	GRCh38
NC_000006.11:g.112390798T= , CM000668.1:g.112390798T=	GRCh37
NC_000006.10:g.112497491T=	NCBI36
NG_011748.1:g.20521T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1040T= MANE Select	ENSP00000357655.4:p.Ile347=
ENST00000639360.1:c.941T=	ENSP00000491774.1:p.Ile314=
ENST00000230529.9:c.1040T=	ENSP00000230529.5:p.Ile347=
ENST00000361714.5:c.1040T=	ENSP00000354734.2:p.Ile347=
ENST00000368663.4:c.*346T=	ENSP00000357652.4:n.*346T=
ENST00000368664.7:c.*444T=	ENSP00000357653.3:n.*444T=
ENST00000368666.6:c.1094T=	ENSP00000357655.3:p.Ile365=
ENST00000409166.5:c.368T=	ENSP00000386467.1:p.Ile123=
ENST00000454589.5:c.*444T=	ENSP00000395928.1:n.*444T=
ENST00000604763.5:c.1040T=	ENSP00000473777.1:p.Ile347=
ENST00000613648.1:n.875T=
ENST00000620524.3:n.971T=
NM_003880.3:c.1040T=	NP_003871.1:p.Ile347=
NM_198239.1:c.1094T=	NP_937882.1:p.Ile365=
NR_125353.1:n.1294T=
NR_125354.1:n.1214T=
XM_011536220.1:c.1040T=	XP_011534522.1:p.Ile347=
XM_011536221.1:c.*444T=	XP_011534523.1:n.*444T=
XM_011536223.1:c.458T=	XP_011534525.1:p.Ile153=
XM_011536223.3:c.458T=	XP_011534525.1:p.Ile153=
XR_001743705.1:n.1642T=
NM_003880.4:c.1040T=	NP_003871.1:p.Ile347=
NM_198239.2:c.1040T= MANE Select	NP_937882.2:p.Ile347=
NR_125353.2:n.1358T=
NR_125354.3:n.1185T=