Canonical Allele Identifier: CA365376125

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390651T>G (hg19) ; chr6:g.112069448T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069448T>G , CM000668.2:g.112069448T>G	GRCh38
NC_000006.11:g.112390651T>G , CM000668.1:g.112390651T>G	GRCh37
NC_000006.10:g.112497344T>G	NCBI36
NG_011748.1:g.20374T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.893T>G MANE Select	ENSP00000357655.4:p.Ile298Arg
ENST00000639360.1:c.794T>G	ENSP00000491774.1:p.Ile265Arg
ENST00000230529.9:c.893T>G	ENSP00000230529.5:p.Ile298Arg
ENST00000361714.5:c.893T>G	ENSP00000354734.2:p.Ile298Arg
ENST00000368663.4:c.*199T>G	ENSP00000357652.4:n.*199T>G
ENST00000368664.7:c.*297T>G	ENSP00000357653.3:n.*297T>G
ENST00000368666.6:c.947T>G	ENSP00000357655.3:p.Ile316Arg
ENST00000409166.5:c.221T>G	ENSP00000386467.1:p.Ile74Arg
ENST00000454589.5:c.*297T>G	ENSP00000395928.1:n.*297T>G
ENST00000604763.5:c.893T>G	ENSP00000473777.1:p.Ile298Arg
ENST00000613648.1:n.728T>G
ENST00000620524.3:n.824T>G
NM_003880.3:c.893T>G	NP_003871.1:p.Ile298Arg
NM_198239.1:c.947T>G	NP_937882.1:p.Ile316Arg
NR_125353.1:n.1147T>G
NR_125354.1:n.1067T>G
XM_011536220.1:c.893T>G	XP_011534522.1:p.Ile298Arg
XM_011536221.1:c.*297T>G	XP_011534523.1:n.*297T>G
XM_011536223.1:c.311T>G	XP_011534525.1:p.Ile104Arg
XM_011536223.3:c.311T>G	XP_011534525.1:p.Ile104Arg
XR_001743705.1:n.1495T>G
NM_003880.4:c.893T>G	NP_003871.1:p.Ile298Arg
NM_198239.2:c.893T>G MANE Select	NP_937882.2:p.Ile298Arg
NR_125353.2:n.1211T>G
NR_125354.3:n.1038T>G