Canonical Allele Identifier: CA451598961

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390823A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069620A>G , CM000668.2:g.112069620A>G	GRCh38
NC_000006.11:g.112390823A>G , CM000668.1:g.112390823A>G	GRCh37
NC_000006.10:g.112497516A>G	NCBI36
NG_011748.1:g.20546A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1065A>G MANE Select	ENSP00000357655.4:p.Ter355=
ENST00000639360.1:c.966A>G	ENSP00000491774.1:p.Ter322=
ENST00000230529.9:c.1065A>G	ENSP00000230529.5:p.Ter355=
ENST00000361714.5:c.1065A>G	ENSP00000354734.2:p.Ter355=
ENST00000368663.4:c.*371A>G	ENSP00000357652.4:n.*371A>G
ENST00000368664.7:c.*469A>G	ENSP00000357653.3:n.*469A>G
ENST00000368666.6:c.1119A>G	ENSP00000357655.3:p.Ter373=
ENST00000409166.5:c.393A>G	ENSP00000386467.1:p.Ter131=
ENST00000454589.5:c.*469A>G	ENSP00000395928.1:n.*469A>G
ENST00000604763.5:c.1065A>G	ENSP00000473777.1:p.Ter355=
ENST00000613648.1:n.900A>G
ENST00000620524.3:n.996A>G
NM_003880.3:c.1065A>G	NP_003871.1:p.Ter355=
NM_198239.1:c.1119A>G	NP_937882.1:p.Ter373=
NR_125353.1:n.1319A>G
NR_125354.1:n.1239A>G
XM_011536220.1:c.1065A>G	XP_011534522.1:p.Ter355=
XM_011536221.1:c.*469A>G	XP_011534523.1:n.*469A>G
XM_011536223.1:c.483A>G	XP_011534525.1:p.Ter161=
XM_011536223.3:c.483A>G	XP_011534525.1:p.Ter161=
XR_001743705.1:n.1667A>G
NM_003880.4:c.1065A>G	NP_003871.1:p.Ter355=
NM_198239.2:c.1065A>G MANE Select	NP_937882.2:p.Ter355=
NR_125353.2:n.1383A>G
NR_125354.3:n.1210A>G