Canonical Allele Identifier: CA365376877
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069575C>G , CM000668.2:g.112069575C>G GRCh38
NC_000006.11:g.112390778C>G , CM000668.1:g.112390778C>G GRCh37
NC_000006.10:g.112497471C>G NCBI36
NG_011748.1:g.20501C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000368666.7:c.1020C>G MANE Select ENSP00000357655.4:p.Asn340Lys
ENST00000639360.1:c.921C>G ENSP00000491774.1:p.Asn307Lys
ENST00000230529.9:c.1020C>G ENSP00000230529.5:p.Asn340Lys
ENST00000361714.5:c.1020C>G ENSP00000354734.2:p.Asn340Lys
ENST00000368663.4:c.*326C>G ENSP00000357652.4:n.*326C>G
ENST00000368664.7:c.*424C>G ENSP00000357653.3:n.*424C>G
ENST00000368666.6:c.1074C>G ENSP00000357655.3:p.Asn358Lys
ENST00000409166.5:c.348C>G ENSP00000386467.1:p.Asn116Lys
ENST00000454589.5:c.*424C>G ENSP00000395928.1:n.*424C>G
ENST00000604763.5:c.1020C>G ENSP00000473777.1:p.Asn340Lys
ENST00000613648.1:n.855C>G
ENST00000620524.3:n.951C>G
NM_003880.3:c.1020C>G NP_003871.1:p.Asn340Lys
NM_198239.1:c.1074C>G NP_937882.1:p.Asn358Lys
NR_125353.1:n.1274C>G
NR_125354.1:n.1194C>G
XM_011536220.1:c.1020C>G XP_011534522.1:p.Asn340Lys
XM_011536221.1:c.*424C>G XP_011534523.1:n.*424C>G
XM_011536223.1:c.438C>G XP_011534525.1:p.Asn146Lys
XM_011536223.3:c.438C>G XP_011534525.1:p.Asn146Lys
XR_001743705.1:n.1622C>G
NM_003880.4:c.1020C>G NP_003871.1:p.Asn340Lys
NM_198239.2:c.1020C>G MANE Select NP_937882.2:p.Asn340Lys
NR_125353.2:n.1338C>G
NR_125354.3:n.1165C>G