Canonical Allele Identifier: CA3964140
Gene: CCN6 HGNC NCBI

Linked Data

dbSNP Id: rs781986930

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069565G>C , CM000668.2:g.112069565G>C GRCh38
NC_000006.11:g.112390768G>C , CM000668.1:g.112390768G>C GRCh37
NC_000006.10:g.112497461G>C NCBI36
NG_011748.1:g.20491G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000368666.7:c.1010G>C MANE Select ENSP00000357655.4:p.Cys337Ser
ENST00000639360.1:c.911G>C ENSP00000491774.1:p.Cys304Ser
ENST00000230529.9:c.1010G>C ENSP00000230529.5:p.Cys337Ser
ENST00000361714.5:c.1010G>C ENSP00000354734.2:p.Cys337Ser
ENST00000368663.4:c.*316G>C ENSP00000357652.4:n.*316G>C
ENST00000368664.7:c.*414G>C ENSP00000357653.3:n.*414G>C
ENST00000368666.6:c.1064G>C ENSP00000357655.3:p.Cys355Ser
ENST00000409166.5:c.338G>C ENSP00000386467.1:p.Cys113Ser
ENST00000454589.5:c.*414G>C ENSP00000395928.1:n.*414G>C
ENST00000604763.5:c.1010G>C ENSP00000473777.1:p.Cys337Ser
ENST00000613648.1:n.845G>C
ENST00000620524.3:n.941G>C
NM_003880.3:c.1010G>C NP_003871.1:p.Cys337Ser
NM_198239.1:c.1064G>C NP_937882.1:p.Cys355Ser
NR_125353.1:n.1264G>C
NR_125354.1:n.1184G>C
XM_011536220.1:c.1010G>C XP_011534522.1:p.Cys337Ser
XM_011536221.1:c.*414G>C XP_011534523.1:n.*414G>C
XM_011536223.1:c.428G>C XP_011534525.1:p.Cys143Ser
XM_011536223.3:c.428G>C XP_011534525.1:p.Cys143Ser
XR_001743705.1:n.1612G>C
NM_003880.4:c.1010G>C NP_003871.1:p.Cys337Ser
NM_198239.2:c.1010G>C MANE Select NP_937882.2:p.Cys337Ser
NR_125353.2:n.1328G>C
NR_125354.3:n.1155G>C