Canonical Allele Identifier: CA1655201619

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069635G= , CM000668.2:g.112069635G=	GRCh38
NC_000006.11:g.112390838G= , CM000668.1:g.112390838G=	GRCh37
NC_000006.10:g.112497531G=	NCBI36
NG_011748.1:g.20561G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*15G= MANE Select	ENSP00000357655.4:n.*15G=
ENST00000639360.1:c.981G=	ENSP00000491774.1:n.981G=
ENST00000230529.9:c.*15G=	ENSP00000230529.5:n.*15G=
ENST00000361714.5:c.*15G=	ENSP00000354734.2:n.*15G=
ENST00000368663.4:c.*386G=	ENSP00000357652.4:n.*386G=
ENST00000368664.7:c.*484G=	ENSP00000357653.3:n.*484G=
ENST00000368666.6:c.*15G=	ENSP00000357655.3:n.*15G=
ENST00000409166.5:c.*15G=	ENSP00000386467.1:n.*15G=
ENST00000454589.5:c.*484G=	ENSP00000395928.1:n.*484G=
ENST00000604763.5:c.*15G=	ENSP00000473777.1:n.*15G=
ENST00000613648.1:n.915G=
ENST00000620524.3:n.1011G=
NM_003880.3:c.*15G=	NP_003871.1:n.*15G=
NM_198239.1:c.*15G=	NP_937882.1:n.*15G=
NR_125353.1:n.1334G=
NR_125354.1:n.1254G=
XM_011536220.1:c.*15G=	XP_011534522.1:n.*15G=
XM_011536221.1:c.*484G=	XP_011534523.1:n.*484G=
XM_011536223.1:c.*15G=	XP_011534525.1:n.*15G=
XM_011536223.3:c.*15G=	XP_011534525.1:n.*15G=
XR_001743705.1:n.1682G=
NM_003880.4:c.*15G=	NP_003871.1:n.*15G=
NM_198239.2:c.*15G= MANE Select	NP_937882.2:n.*15G=
NR_125353.2:n.1398G=
NR_125354.3:n.1225G=