Canonical Allele Identifier: CA365376887

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390780G>A (hg19) ; chr6:g.112069577G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069577G>A , CM000668.2:g.112069577G>A	GRCh38
NC_000006.11:g.112390780G>A , CM000668.1:g.112390780G>A	GRCh37
NC_000006.10:g.112497473G>A	NCBI36
NG_011748.1:g.20503G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1022G>A MANE Select	ENSP00000357655.4:p.Cys341Tyr
ENST00000639360.1:c.923G>A	ENSP00000491774.1:p.Cys308Tyr
ENST00000230529.9:c.1022G>A	ENSP00000230529.5:p.Cys341Tyr
ENST00000361714.5:c.1022G>A	ENSP00000354734.2:p.Cys341Tyr
ENST00000368663.4:c.*328G>A	ENSP00000357652.4:n.*328G>A
ENST00000368664.7:c.*426G>A	ENSP00000357653.3:n.*426G>A
ENST00000368666.6:c.1076G>A	ENSP00000357655.3:p.Cys359Tyr
ENST00000409166.5:c.350G>A	ENSP00000386467.1:p.Cys117Tyr
ENST00000454589.5:c.*426G>A	ENSP00000395928.1:n.*426G>A
ENST00000604763.5:c.1022G>A	ENSP00000473777.1:p.Cys341Tyr
ENST00000613648.1:n.857G>A
ENST00000620524.3:n.953G>A
NM_003880.3:c.1022G>A	NP_003871.1:p.Cys341Tyr
NM_198239.1:c.1076G>A	NP_937882.1:p.Cys359Tyr
NR_125353.1:n.1276G>A
NR_125354.1:n.1196G>A
XM_011536220.1:c.1022G>A	XP_011534522.1:p.Cys341Tyr
XM_011536221.1:c.*426G>A	XP_011534523.1:n.*426G>A
XM_011536223.1:c.440G>A	XP_011534525.1:p.Cys147Tyr
XM_011536223.3:c.440G>A	XP_011534525.1:p.Cys147Tyr
XR_001743705.1:n.1624G>A
NM_003880.4:c.1022G>A	NP_003871.1:p.Cys341Tyr
NM_198239.2:c.1022G>A MANE Select	NP_937882.2:p.Cys341Tyr
NR_125353.2:n.1340G>A
NR_125354.3:n.1167G>A