Canonical Allele Identifier: CA2695206927

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069441dup , CM000668.2:g.112069441dup	GRCh38
NC_000006.11:g.112390644dup , CM000668.1:g.112390644dup	GRCh37
NC_000006.10:g.112497337dup	NCBI36
NG_011748.1:g.20367dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.886dup MANE Select	ENSP00000357655.4:p.Cys296LeufsTer7
ENST00000639360.1:c.787dup	ENSP00000491774.1:p.Cys263LeufsTer7
ENST00000230529.9:c.886dup	ENSP00000230529.5:p.Cys296LeufsTer7
ENST00000361714.5:c.886dup	ENSP00000354734.2:p.Cys296LeufsTer7
ENST00000368663.4:c.*192dup	ENSP00000357652.4:n.*192dup
ENST00000368664.7:c.*290dup	ENSP00000357653.3:n.*290dup
ENST00000368666.6:c.940dup	ENSP00000357655.3:p.Cys314LeufsTer7
ENST00000409166.5:c.214dup	ENSP00000386467.1:p.Cys72LeufsTer7
ENST00000454589.5:c.*290dup	ENSP00000395928.1:n.*290dup
ENST00000604763.5:c.886dup	ENSP00000473777.1:p.Cys296LeufsTer7
ENST00000613648.1:n.721dup
ENST00000620524.3:n.817dup
NM_003880.3:c.886dup	NP_003871.1:p.Cys296LeufsTer7
NM_198239.1:c.940dup	NP_937882.1:p.Cys314LeufsTer7
NR_125353.1:n.1140dup
NR_125354.1:n.1060dup
XM_011536220.1:c.886dup	XP_011534522.1:p.Cys296LeufsTer7
XM_011536221.1:c.*290dup	XP_011534523.1:n.*290dup
XM_011536223.1:c.304dup	XP_011534525.1:p.Cys102LeufsTer7
XM_011536223.3:c.304dup	XP_011534525.1:p.Cys102LeufsTer7
XR_001743705.1:n.1488dup
NM_003880.4:c.886dup	NP_003871.1:p.Cys296LeufsTer7
NM_198239.2:c.886dup MANE Select	NP_937882.2:p.Cys296LeufsTer7
NR_125353.2:n.1204dup
NR_125354.3:n.1031dup