Canonical Allele Identifier: CA365376298
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069481A>G , CM000668.2:g.112069481A>G GRCh38
NC_000006.11:g.112390684A>G , CM000668.1:g.112390684A>G GRCh37
NC_000006.10:g.112497377A>G NCBI36
NG_011748.1:g.20407A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368666.7:c.926A>G MANE Select ENSP00000357655.4:p.Lys309Arg
ENST00000639360.1:c.827A>G ENSP00000491774.1:p.Lys276Arg
ENST00000230529.9:c.926A>G ENSP00000230529.5:p.Lys309Arg
ENST00000361714.5:c.926A>G ENSP00000354734.2:p.Lys309Arg
ENST00000368663.4:c.*232A>G ENSP00000357652.4:n.*232A>G
ENST00000368664.7:c.*330A>G ENSP00000357653.3:n.*330A>G
ENST00000368666.6:c.980A>G ENSP00000357655.3:p.Lys327Arg
ENST00000409166.5:c.254A>G ENSP00000386467.1:p.Lys85Arg
ENST00000454589.5:c.*330A>G ENSP00000395928.1:n.*330A>G
ENST00000604763.5:c.926A>G ENSP00000473777.1:p.Lys309Arg
ENST00000613648.1:n.761A>G
ENST00000620524.3:n.857A>G
NM_003880.3:c.926A>G NP_003871.1:p.Lys309Arg
NM_198239.1:c.980A>G NP_937882.1:p.Lys327Arg
NR_125353.1:n.1180A>G
NR_125354.1:n.1100A>G
XM_011536220.1:c.926A>G XP_011534522.1:p.Lys309Arg
XM_011536221.1:c.*330A>G XP_011534523.1:n.*330A>G
XM_011536223.1:c.344A>G XP_011534525.1:p.Lys115Arg
XM_011536223.3:c.344A>G XP_011534525.1:p.Lys115Arg
XR_001743705.1:n.1528A>G
NM_003880.4:c.926A>G NP_003871.1:p.Lys309Arg
NM_198239.2:c.926A>G MANE Select NP_937882.2:p.Lys309Arg
NR_125353.2:n.1244A>G
NR_125354.3:n.1071A>G