Canonical Allele Identifier: CA1655201614

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069613T= , CM000668.2:g.112069613T=	GRCh38
NC_000006.11:g.112390816T= , CM000668.1:g.112390816T=	GRCh37
NC_000006.10:g.112497509T=	NCBI36
NG_011748.1:g.20539T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1058T= MANE Select	ENSP00000357655.4:p.Ile353=
ENST00000639360.1:c.959T=	ENSP00000491774.1:p.Ile320=
ENST00000230529.9:c.1058T=	ENSP00000230529.5:p.Ile353=
ENST00000361714.5:c.1058T=	ENSP00000354734.2:p.Ile353=
ENST00000368663.4:c.*364T=	ENSP00000357652.4:n.*364T=
ENST00000368664.7:c.*462T=	ENSP00000357653.3:n.*462T=
ENST00000368666.6:c.1112T=	ENSP00000357655.3:p.Ile371=
ENST00000409166.5:c.386T=	ENSP00000386467.1:p.Ile129=
ENST00000454589.5:c.*462T=	ENSP00000395928.1:n.*462T=
ENST00000604763.5:c.1058T=	ENSP00000473777.1:p.Ile353=
ENST00000613648.1:n.893T=
ENST00000620524.3:n.989T=
NM_003880.3:c.1058T=	NP_003871.1:p.Ile353=
NM_198239.1:c.1112T=	NP_937882.1:p.Ile371=
NR_125353.1:n.1312T=
NR_125354.1:n.1232T=
XM_011536220.1:c.1058T=	XP_011534522.1:p.Ile353=
XM_011536221.1:c.*462T=	XP_011534523.1:n.*462T=
XM_011536223.1:c.476T=	XP_011534525.1:p.Ile159=
XM_011536223.3:c.476T=	XP_011534525.1:p.Ile159=
XR_001743705.1:n.1660T=
NM_003880.4:c.1058T=	NP_003871.1:p.Ile353=
NM_198239.2:c.1058T= MANE Select	NP_937882.2:p.Ile353=
NR_125353.2:n.1376T=
NR_125354.3:n.1203T=