Canonical Allele Identifier: CA365376928
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069582G>A , CM000668.2:g.112069582G>A GRCh38
NC_000006.11:g.112390785G>A , CM000668.1:g.112390785G>A GRCh37
NC_000006.10:g.112497478G>A NCBI36
NG_011748.1:g.20508G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368666.7:c.1027G>A MANE Select ENSP00000357655.4:p.Glu343Lys
ENST00000639360.1:c.928G>A ENSP00000491774.1:p.Glu310Lys
ENST00000230529.9:c.1027G>A ENSP00000230529.5:p.Glu343Lys
ENST00000361714.5:c.1027G>A ENSP00000354734.2:p.Glu343Lys
ENST00000368663.4:c.*333G>A ENSP00000357652.4:n.*333G>A
ENST00000368664.7:c.*431G>A ENSP00000357653.3:n.*431G>A
ENST00000368666.6:c.1081G>A ENSP00000357655.3:p.Glu361Lys
ENST00000409166.5:c.355G>A ENSP00000386467.1:p.Glu119Lys
ENST00000454589.5:c.*431G>A ENSP00000395928.1:n.*431G>A
ENST00000604763.5:c.1027G>A ENSP00000473777.1:p.Glu343Lys
ENST00000613648.1:n.862G>A
ENST00000620524.3:n.958G>A
NM_003880.3:c.1027G>A NP_003871.1:p.Glu343Lys
NM_198239.1:c.1081G>A NP_937882.1:p.Glu361Lys
NR_125353.1:n.1281G>A
NR_125354.1:n.1201G>A
XM_011536220.1:c.1027G>A XP_011534522.1:p.Glu343Lys
XM_011536221.1:c.*431G>A XP_011534523.1:n.*431G>A
XM_011536223.1:c.445G>A XP_011534525.1:p.Glu149Lys
XM_011536223.3:c.445G>A XP_011534525.1:p.Glu149Lys
XR_001743705.1:n.1629G>A
NM_003880.4:c.1027G>A NP_003871.1:p.Glu343Lys
NM_198239.2:c.1027G>A MANE Select NP_937882.2:p.Glu343Lys
NR_125353.2:n.1345G>A
NR_125354.3:n.1172G>A