Canonical Allele Identifier: CA1655201590

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069552A= , CM000668.2:g.112069552A=	GRCh38
NC_000006.11:g.112390755A= , CM000668.1:g.112390755A=	GRCh37
NC_000006.10:g.112497448A=	NCBI36
NG_011748.1:g.20478A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.997A= MANE Select	ENSP00000357655.4:p.Thr333=
ENST00000639360.1:c.898A=	ENSP00000491774.1:p.Thr300=
ENST00000230529.9:c.997A=	ENSP00000230529.5:p.Thr333=
ENST00000361714.5:c.997A=	ENSP00000354734.2:p.Thr333=
ENST00000368663.4:c.*303A=	ENSP00000357652.4:n.*303A=
ENST00000368664.7:c.*401A=	ENSP00000357653.3:n.*401A=
ENST00000368666.6:c.1051A=	ENSP00000357655.3:p.Thr351=
ENST00000409166.5:c.325A=	ENSP00000386467.1:p.Thr109=
ENST00000454589.5:c.*401A=	ENSP00000395928.1:n.*401A=
ENST00000604763.5:c.997A=	ENSP00000473777.1:p.Thr333=
ENST00000613648.1:n.832A=
ENST00000620524.3:n.928A=
NM_003880.3:c.997A=	NP_003871.1:p.Thr333=
NM_198239.1:c.1051A=	NP_937882.1:p.Thr351=
NR_125353.1:n.1251A=
NR_125354.1:n.1171A=
XM_011536220.1:c.997A=	XP_011534522.1:p.Thr333=
XM_011536221.1:c.*401A=	XP_011534523.1:n.*401A=
XM_011536223.1:c.415A=	XP_011534525.1:p.Thr139=
XM_011536223.3:c.415A=	XP_011534525.1:p.Thr139=
XR_001743705.1:n.1599A=
NM_003880.4:c.997A=	NP_003871.1:p.Thr333=
NM_198239.2:c.997A= MANE Select	NP_937882.2:p.Thr333=
NR_125353.2:n.1315A=
NR_125354.3:n.1142A=