Canonical Allele Identifier: CA1655201602

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069578C= , CM000668.2:g.112069578C=	GRCh38
NC_000006.11:g.112390781C= , CM000668.1:g.112390781C=	GRCh37
NC_000006.10:g.112497474C=	NCBI36
NG_011748.1:g.20504C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1023C= MANE Select	ENSP00000357655.4:p.Cys341=
ENST00000639360.1:c.924C=	ENSP00000491774.1:p.Cys308=
ENST00000230529.9:c.1023C=	ENSP00000230529.5:p.Cys341=
ENST00000361714.5:c.1023C=	ENSP00000354734.2:p.Cys341=
ENST00000368663.4:c.*329C=	ENSP00000357652.4:n.*329C=
ENST00000368664.7:c.*427C=	ENSP00000357653.3:n.*427C=
ENST00000368666.6:c.1077C=	ENSP00000357655.3:p.Cys359=
ENST00000409166.5:c.351C=	ENSP00000386467.1:p.Cys117=
ENST00000454589.5:c.*427C=	ENSP00000395928.1:n.*427C=
ENST00000604763.5:c.1023C=	ENSP00000473777.1:p.Cys341=
ENST00000613648.1:n.858C=
ENST00000620524.3:n.954C=
NM_003880.3:c.1023C=	NP_003871.1:p.Cys341=
NM_198239.1:c.1077C=	NP_937882.1:p.Cys359=
NR_125353.1:n.1277C=
NR_125354.1:n.1197C=
XM_011536220.1:c.1023C=	XP_011534522.1:p.Cys341=
XM_011536221.1:c.*427C=	XP_011534523.1:n.*427C=
XM_011536223.1:c.441C=	XP_011534525.1:p.Cys147=
XM_011536223.3:c.441C=	XP_011534525.1:p.Cys147=
XR_001743705.1:n.1625C=
NM_003880.4:c.1023C=	NP_003871.1:p.Cys341=
NM_198239.2:c.1023C= MANE Select	NP_937882.2:p.Cys341=
NR_125353.2:n.1341C=
NR_125354.3:n.1168C=