Canonical Allele Identifier: CA1655201621

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069638A= , CM000668.2:g.112069638A=	GRCh38
NC_000006.11:g.112390841A= , CM000668.1:g.112390841A=	GRCh37
NC_000006.10:g.112497534A=	NCBI36
NG_011748.1:g.20564A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*18A= MANE Select	ENSP00000357655.4:n.*18A=
ENST00000639360.1:c.984A=	ENSP00000491774.1:n.984A=
ENST00000230529.9:c.*18A=	ENSP00000230529.5:n.*18A=
ENST00000361714.5:c.*18A=	ENSP00000354734.2:n.*18A=
ENST00000368663.4:c.*389A=	ENSP00000357652.4:n.*389A=
ENST00000368664.7:c.*487A=	ENSP00000357653.3:n.*487A=
ENST00000368666.6:c.*18A=	ENSP00000357655.3:n.*18A=
ENST00000409166.5:c.*18A=	ENSP00000386467.1:n.*18A=
ENST00000454589.5:c.*487A=	ENSP00000395928.1:n.*487A=
ENST00000604763.5:c.*18A=	ENSP00000473777.1:n.*18A=
ENST00000613648.1:n.918A=
ENST00000620524.3:n.1014A=
NM_003880.3:c.*18A=	NP_003871.1:n.*18A=
NM_198239.1:c.*18A=	NP_937882.1:n.*18A=
NR_125353.1:n.1337A=
NR_125354.1:n.1257A=
XM_011536220.1:c.*18A=	XP_011534522.1:n.*18A=
XM_011536221.1:c.*487A=	XP_011534523.1:n.*487A=
XM_011536223.1:c.*18A=	XP_011534525.1:n.*18A=
XM_011536223.3:c.*18A=	XP_011534525.1:n.*18A=
XR_001743705.1:n.1685A=
NM_003880.4:c.*18A=	NP_003871.1:n.*18A=
NM_198239.2:c.*18A= MANE Select	NP_937882.2:n.*18A=
NR_125353.2:n.1401A=
NR_125354.3:n.1228A=