Canonical Allele Identifier: CA1655201618

Gene: CCN6

Linked Data

• dbSNP Id: rs1562600083
• gnomAD v4: 6-112069627-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069627G>A , CM000668.2:g.112069627G>A	GRCh38
NC_000006.11:g.112390830G>A , CM000668.1:g.112390830G>A	GRCh37
NC_000006.10:g.112497523G>A	NCBI36
NG_011748.1:g.20553G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*7G>A MANE Select	ENSP00000357655.4:n.*7G>A
ENST00000639360.1:c.973G>A	ENSP00000491774.1:n.973G>A
ENST00000230529.9:c.*7G>A	ENSP00000230529.5:n.*7G>A
ENST00000361714.5:c.*7G>A	ENSP00000354734.2:n.*7G>A
ENST00000368663.4:c.*378G>A	ENSP00000357652.4:n.*378G>A
ENST00000368664.7:c.*476G>A	ENSP00000357653.3:n.*476G>A
ENST00000368666.6:c.*7G>A	ENSP00000357655.3:n.*7G>A
ENST00000409166.5:c.*7G>A	ENSP00000386467.1:n.*7G>A
ENST00000454589.5:c.*476G>A	ENSP00000395928.1:n.*476G>A
ENST00000604763.5:c.*7G>A	ENSP00000473777.1:n.*7G>A
ENST00000613648.1:n.907G>A
ENST00000620524.3:n.1003G>A
NM_003880.3:c.*7G>A	NP_003871.1:n.*7G>A
NM_198239.1:c.*7G>A	NP_937882.1:n.*7G>A
NR_125353.1:n.1326G>A
NR_125354.1:n.1246G>A
XM_011536220.1:c.*7G>A	XP_011534522.1:n.*7G>A
XM_011536221.1:c.*476G>A	XP_011534523.1:n.*476G>A
XM_011536223.1:c.*7G>A	XP_011534525.1:n.*7G>A
XM_011536223.3:c.*7G>A	XP_011534525.1:n.*7G>A
XR_001743705.1:n.1674G>A
NM_003880.4:c.*7G>A	NP_003871.1:n.*7G>A
NM_198239.2:c.*7G>A MANE Select	NP_937882.2:n.*7G>A
NR_125353.2:n.1390G>A
NR_125354.3:n.1217G>A