Canonical Allele Identifier: CA2680044652

Gene: CCN6

Linked Data

• ClinVar Variation Id: 2788760
• ClinVar RCV Id: RCV003674277
• gnomAD v4: 6-112060977-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112060977A>G , CM000668.2:g.112060977A>G	GRCh38
NC_000006.11:g.112382180A>G , CM000668.1:g.112382180A>G	GRCh37
NC_000006.10:g.112488873A>G	NCBI36
NG_011748.1:g.11903A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.49-14A>G MANE Select	ENSP00000357655.4:n.49-14A>G
ENST00000230529.9:c.49-14A>G	ENSP00000230529.5:n.49-14A>G
ENST00000361714.5:c.49-14A>G	ENSP00000354734.2:n.49-14A>G
ENST00000368663.4:c.49-14A>G	ENSP00000357652.4:n.49-14A>G
ENST00000368664.7:c.103-14A>G	ENSP00000357653.3:n.103-14A>G
ENST00000368666.6:c.103-14A>G	ENSP00000357655.3:n.103-14A>G
ENST00000409166.5:c.-507-302A>G	ENSP00000386467.1:n.-507-302A>G
ENST00000454589.5:c.49-14A>G	ENSP00000395928.1:n.49-14A>G
ENST00000604763.5:c.49-14A>G	ENSP00000473777.1:n.49-14A>G
ENST00000620524.3:n.64-95A>G
NM_003880.3:c.49-14A>G	NP_003871.1:n.49-14A>G
NM_198239.1:c.103-14A>G	NP_937882.1:n.103-14A>G
NR_125353.1:n.239-14A>G
NR_125354.1:n.159-14A>G
XM_011536220.1:c.49-14A>G	XP_011534522.1:n.49-14A>G
XM_011536221.1:c.112-14A>G	XP_011534523.1:n.112-14A>G
XM_011536222.1:c.187-14A>G	XP_011534524.1:n.187-14A>G
XM_011536222.2:c.112-14A>G	XP_011534524.2:n.112-14A>G
XR_001743705.1:n.587-14A>G
NM_003880.4:c.49-14A>G	NP_003871.1:n.49-14A>G
NM_198239.2:c.49-14A>G MANE Select	NP_937882.2:n.49-14A>G
NR_125353.2:n.303-14A>G
NR_125354.3:n.130-14A>G