Canonical Allele Identifier: CA10585946

Gene: CCN6

Linked Data

• ClinVar Variation Id: 252451
• ClinVar RCV Id: RCV000239146
• dbSNP Id: rs879255273
• MyVariant Identifiers: chr6:g.112386201G>A (hg19) ; chr6:g.112064998G>A (hg38)
• PubMed: PMID:20700952 ; PMID:27291587

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112064998G>A , CM000668.2:g.112064998G>A	GRCh38
NC_000006.11:g.112386201G>A , CM000668.1:g.112386201G>A	GRCh37
NC_000006.10:g.112492894G>A	NCBI36
NG_011748.1:g.15924G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.589+1G>A MANE Select	ENSP00000357655.4:n.589+1G>A
ENST00000639360.1:c.490+1G>A	ENSP00000491774.1:n.490+1G>A
ENST00000230529.9:c.589+1G>A	ENSP00000230529.5:n.589+1G>A
ENST00000361714.5:c.589+1G>A	ENSP00000354734.2:n.589+1G>A
ENST00000368663.4:c.589+1G>A	ENSP00000357652.4:n.589+1G>A
ENST00000368664.7:c.643+1G>A	ENSP00000357653.3:n.643+1G>A
ENST00000368666.6:c.643+1G>A	ENSP00000357655.3:n.643+1G>A
ENST00000409166.5:c.-148+1G>A	ENSP00000386467.1:n.-148+1G>A
ENST00000454589.5:c.589+1G>A	ENSP00000395928.1:n.589+1G>A
ENST00000604763.5:c.589+1G>A	ENSP00000473777.1:n.589+1G>A
ENST00000613648.1:n.360+1G>A
ENST00000620524.3:n.520+1G>A
NM_003880.3:c.589+1G>A	NP_003871.1:n.589+1G>A
NM_198239.1:c.643+1G>A	NP_937882.1:n.643+1G>A
NR_125353.1:n.779+1G>A
NR_125354.1:n.699+1G>A
XM_011536220.1:c.589+1G>A	XP_011534522.1:n.589+1G>A
XM_011536221.1:c.652+1G>A	XP_011534523.1:n.652+1G>A
XM_011536222.1:c.516+212G>A	XP_011534524.1:n.516+212G>A
XM_011536223.1:c.7+1G>A	XP_011534525.1:n.7+1G>A
XM_011536222.2:c.441+212G>A	XP_011534524.2:n.441+212G>A
XM_011536223.3:c.7+1G>A	XP_011534525.1:n.7+1G>A
XR_001743705.1:n.1127+1G>A
NM_003880.4:c.589+1G>A	NP_003871.1:n.589+1G>A
NM_198239.2:c.589+1G>A MANE Select	NP_937882.2:n.589+1G>A
NR_125353.2:n.843+1G>A
NR_125354.3:n.670+1G>A