Canonical Allele Identifier: CA817273894

Gene: CCN6

Linked Data

• dbSNP Id: rs782653530
• MyVariant Identifiers: chr6:g.112390859T>A (hg19) ; chr6:g.112069656T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069656T>A , CM000668.2:g.112069656T>A	GRCh38
NC_000006.11:g.112390859T>A , CM000668.1:g.112390859T>A	GRCh37
NC_000006.10:g.112497552T>A	NCBI36
NG_011748.1:g.20582T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*36T>A MANE Select	ENSP00000357655.4:n.*36T>A
ENST00000639360.1:c.1002T>A	ENSP00000491774.1:n.1002T>A
ENST00000230529.9:c.*36T>A	ENSP00000230529.5:n.*36T>A
ENST00000361714.5:c.*36T>A	ENSP00000354734.2:n.*36T>A
ENST00000368664.7:c.*505T>A	ENSP00000357653.3:n.*505T>A
ENST00000368666.6:c.*36T>A	ENSP00000357655.3:n.*36T>A
ENST00000409166.5:c.*36T>A	ENSP00000386467.1:n.*36T>A
ENST00000454589.5:c.*505T>A	ENSP00000395928.1:n.*505T>A
ENST00000604763.5:c.*36T>A	ENSP00000473777.1:n.*36T>A
ENST00000613648.1:n.936T>A
ENST00000620524.3:n.1032T>A
NM_003880.3:c.*36T>A	NP_003871.1:n.*36T>A
NM_198239.1:c.*36T>A	NP_937882.1:n.*36T>A
NR_125353.1:n.1355T>A
NR_125354.1:n.1275T>A
XM_011536220.1:c.*36T>A	XP_011534522.1:n.*36T>A
XM_011536221.1:c.*505T>A	XP_011534523.1:n.*505T>A
XM_011536223.1:c.*36T>A	XP_011534525.1:n.*36T>A
XM_011536223.3:c.*36T>A	XP_011534525.1:n.*36T>A
XR_001743705.1:n.1703T>A
NM_003880.4:c.*36T>A	NP_003871.1:n.*36T>A
NM_198239.2:c.*36T>A MANE Select	NP_937882.2:n.*36T>A
NR_125353.2:n.1419T>A
NR_125354.3:n.1246T>A