Canonical Allele Identifier: CA451901323

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390637C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069434C>A , CM000668.2:g.112069434C>A	GRCh38
NC_000006.11:g.112390637C>A , CM000668.1:g.112390637C>A	GRCh37
NC_000006.10:g.112497330C>A	NCBI36
NG_011748.1:g.20360C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.879C>A MANE Select	ENSP00000357655.4:p.Pro293=
ENST00000639360.1:c.780C>A	ENSP00000491774.1:p.Pro260=
ENST00000230529.9:c.879C>A	ENSP00000230529.5:p.Pro293=
ENST00000361714.5:c.879C>A	ENSP00000354734.2:p.Pro293=
ENST00000368663.4:c.*185C>A	ENSP00000357652.4:n.*185C>A
ENST00000368664.7:c.*283C>A	ENSP00000357653.3:n.*283C>A
ENST00000368666.6:c.933C>A	ENSP00000357655.3:p.Pro311=
ENST00000409166.5:c.207C>A	ENSP00000386467.1:p.Pro69=
ENST00000454589.5:c.*283C>A	ENSP00000395928.1:n.*283C>A
ENST00000604763.5:c.879C>A	ENSP00000473777.1:p.Pro293=
ENST00000613648.1:n.714C>A
ENST00000620524.3:n.810C>A
NM_003880.3:c.879C>A	NP_003871.1:p.Pro293=
NM_198239.1:c.933C>A	NP_937882.1:p.Pro311=
NR_125353.1:n.1133C>A
NR_125354.1:n.1053C>A
XM_011536220.1:c.879C>A	XP_011534522.1:p.Pro293=
XM_011536221.1:c.*283C>A	XP_011534523.1:n.*283C>A
XM_011536223.1:c.297C>A	XP_011534525.1:p.Pro99=
XM_011536223.3:c.297C>A	XP_011534525.1:p.Pro99=
XR_001743705.1:n.1481C>A
NM_003880.4:c.879C>A	NP_003871.1:p.Pro293=
NM_198239.2:c.879C>A MANE Select	NP_937882.2:p.Pro293=
NR_125353.2:n.1197C>A
NR_125354.3:n.1024C>A