Canonical Allele Identifier: CA569670405

Gene: CCN6

Linked Data

• dbSNP Id: rs1554314835
• gnomAD v2: 6-112390873-AATT-A
• MyVariant Identifiers: chr6:g.112390874_112390876del (hg19) ; chr6:g.112069671_112069673del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069672_112069674del , CM000668.2:g.112069672_112069674del	GRCh38
NC_000006.11:g.112390875_112390877del , CM000668.1:g.112390875_112390877del	GRCh37
NC_000006.10:g.112497568_112497570del	NCBI36
NG_011748.1:g.20598_20600del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*52_*54del MANE Select	ENSP00000357655.4:n.*52_*54del
ENST00000639360.1:c.1018_1020del	ENSP00000491774.1:n.1018_1020del
ENST00000230529.9:c.*52_*54del	ENSP00000230529.5:n.*52_*54del
ENST00000361714.5:c.*52_*54del	ENSP00000354734.2:n.*52_*54del
ENST00000368666.6:c.*52_*54del	ENSP00000357655.3:n.*52_*54del
ENST00000454589.5:c.*521_*523del	ENSP00000395928.1:n.*521_*523del
ENST00000604763.5:c.*52_*54del	ENSP00000473777.1:n.*52_*54del
ENST00000620524.3:n.1048_1050del
NM_003880.3:c.*52_*54del	NP_003871.1:n.*52_*54del
NM_198239.1:c.*52_*54del	NP_937882.1:n.*52_*54del
NR_125353.1:n.1371_1373del
NR_125354.1:n.1291_1293del
XM_011536220.1:c.*52_*54del	XP_011534522.1:n.*52_*54del
XM_011536221.1:c.*521_*523del	XP_011534523.1:n.*521_*523del
XM_011536223.1:c.*52_*54del	XP_011534525.1:n.*52_*54del
XM_011536223.3:c.*52_*54del	XP_011534525.1:n.*52_*54del
XR_001743705.1:n.1719_1721del
NM_003880.4:c.*52_*54del	NP_003871.1:n.*52_*54del
NM_198239.2:c.*52_*54del MANE Select	NP_937882.2:n.*52_*54del
NR_125353.2:n.1435_1437del
NR_125354.3:n.1262_1264del