Canonical Allele Identifier: CA1655201644

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069677G= , CM000668.2:g.112069677G=	GRCh38
NC_000006.11:g.112390880G= , CM000668.1:g.112390880G=	GRCh37
NC_000006.10:g.112497573G=	NCBI36
NG_011748.1:g.20603G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*57G= MANE Select	ENSP00000357655.4:n.*57G=
ENST00000639360.1:c.1023G=	ENSP00000491774.1:n.1023G=
ENST00000230529.9:c.*57G=	ENSP00000230529.5:n.*57G=
ENST00000361714.5:c.*57G=	ENSP00000354734.2:n.*57G=
ENST00000368666.6:c.*57G=	ENSP00000357655.3:n.*57G=
ENST00000454589.5:c.*526G=	ENSP00000395928.1:n.*526G=
ENST00000604763.5:c.*57G=	ENSP00000473777.1:n.*57G=
ENST00000620524.3:n.1053G=
NM_003880.3:c.*57G=	NP_003871.1:n.*57G=
NM_198239.1:c.*57G=	NP_937882.1:n.*57G=
NR_125353.1:n.1376G=
NR_125354.1:n.1296G=
XM_011536220.1:c.*57G=	XP_011534522.1:n.*57G=
XM_011536221.1:c.*526G=	XP_011534523.1:n.*526G=
XM_011536223.1:c.*57G=	XP_011534525.1:n.*57G=
XM_011536223.3:c.*57G=	XP_011534525.1:n.*57G=
XR_001743705.1:n.1724G=
NM_003880.4:c.*57G=	NP_003871.1:n.*57G=
NM_198239.2:c.*57G= MANE Select	NP_937882.2:n.*57G=
NR_125353.2:n.1440G=
NR_125354.3:n.1267G=