Canonical Allele Identifier: CA1655201554

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069436C= , CM000668.2:g.112069436C=	GRCh38
NC_000006.11:g.112390639C= , CM000668.1:g.112390639C=	GRCh37
NC_000006.10:g.112497332C=	NCBI36
NG_011748.1:g.20362C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.881C= MANE Select	ENSP00000357655.4:p.Thr294=
ENST00000639360.1:c.782C=	ENSP00000491774.1:p.Thr261=
ENST00000230529.9:c.881C=	ENSP00000230529.5:p.Thr294=
ENST00000361714.5:c.881C=	ENSP00000354734.2:p.Thr294=
ENST00000368663.4:c.*187C=	ENSP00000357652.4:n.*187C=
ENST00000368664.7:c.*285C=	ENSP00000357653.3:n.*285C=
ENST00000368666.6:c.935C=	ENSP00000357655.3:p.Thr312=
ENST00000409166.5:c.209C=	ENSP00000386467.1:p.Thr70=
ENST00000454589.5:c.*285C=	ENSP00000395928.1:n.*285C=
ENST00000604763.5:c.881C=	ENSP00000473777.1:p.Thr294=
ENST00000613648.1:n.716C=
ENST00000620524.3:n.812C=
NM_003880.3:c.881C=	NP_003871.1:p.Thr294=
NM_198239.1:c.935C=	NP_937882.1:p.Thr312=
NR_125353.1:n.1135C=
NR_125354.1:n.1055C=
XM_011536220.1:c.881C=	XP_011534522.1:p.Thr294=
XM_011536221.1:c.*285C=	XP_011534523.1:n.*285C=
XM_011536223.1:c.299C=	XP_011534525.1:p.Thr100=
XM_011536223.3:c.299C=	XP_011534525.1:p.Thr100=
XR_001743705.1:n.1483C=
NM_003880.4:c.881C=	NP_003871.1:p.Thr294=
NM_198239.2:c.881C= MANE Select	NP_937882.2:p.Thr294=
NR_125353.2:n.1199C=
NR_125354.3:n.1026C=