Canonical Allele Identifier: CA1655201625

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069647T= , CM000668.2:g.112069647T=	GRCh38
NC_000006.11:g.112390850T= , CM000668.1:g.112390850T=	GRCh37
NC_000006.10:g.112497543T=	NCBI36
NG_011748.1:g.20573T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*27T= MANE Select	ENSP00000357655.4:n.*27T=
ENST00000639360.1:c.993T=	ENSP00000491774.1:n.993T=
ENST00000230529.9:c.*27T=	ENSP00000230529.5:n.*27T=
ENST00000361714.5:c.*27T=	ENSP00000354734.2:n.*27T=
ENST00000368664.7:c.*496T=	ENSP00000357653.3:n.*496T=
ENST00000368666.6:c.*27T=	ENSP00000357655.3:n.*27T=
ENST00000409166.5:c.*27T=	ENSP00000386467.1:n.*27T=
ENST00000454589.5:c.*496T=	ENSP00000395928.1:n.*496T=
ENST00000604763.5:c.*27T=	ENSP00000473777.1:n.*27T=
ENST00000613648.1:n.927T=
ENST00000620524.3:n.1023T=
NM_003880.3:c.*27T=	NP_003871.1:n.*27T=
NM_198239.1:c.*27T=	NP_937882.1:n.*27T=
NR_125353.1:n.1346T=
NR_125354.1:n.1266T=
XM_011536220.1:c.*27T=	XP_011534522.1:n.*27T=
XM_011536221.1:c.*496T=	XP_011534523.1:n.*496T=
XM_011536223.1:c.*27T=	XP_011534525.1:n.*27T=
XM_011536223.3:c.*27T=	XP_011534525.1:n.*27T=
XR_001743705.1:n.1694T=
NM_003880.4:c.*27T=	NP_003871.1:n.*27T=
NM_198239.2:c.*27T= MANE Select	NP_937882.2:n.*27T=
NR_125353.2:n.1410T=
NR_125354.3:n.1237T=