Canonical Allele Identifier: CA365376890
Gene: CCN6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069578C>A , CM000668.2:g.112069578C>A GRCh38
NC_000006.11:g.112390781C>A , CM000668.1:g.112390781C>A GRCh37
NC_000006.10:g.112497474C>A NCBI36
NG_011748.1:g.20504C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000368666.7:c.1023C>A MANE Select ENSP00000357655.4:p.Cys341Ter
ENST00000639360.1:c.924C>A ENSP00000491774.1:p.Cys308Ter
ENST00000230529.9:c.1023C>A ENSP00000230529.5:p.Cys341Ter
ENST00000361714.5:c.1023C>A ENSP00000354734.2:p.Cys341Ter
ENST00000368663.4:c.*329C>A ENSP00000357652.4:n.*329C>A
ENST00000368664.7:c.*427C>A ENSP00000357653.3:n.*427C>A
ENST00000368666.6:c.1077C>A ENSP00000357655.3:p.Cys359Ter
ENST00000409166.5:c.351C>A ENSP00000386467.1:p.Cys117Ter
ENST00000454589.5:c.*427C>A ENSP00000395928.1:n.*427C>A
ENST00000604763.5:c.1023C>A ENSP00000473777.1:p.Cys341Ter
ENST00000613648.1:n.858C>A
ENST00000620524.3:n.954C>A
NM_003880.3:c.1023C>A NP_003871.1:p.Cys341Ter
NM_198239.1:c.1077C>A NP_937882.1:p.Cys359Ter
NR_125353.1:n.1277C>A
NR_125354.1:n.1197C>A
XM_011536220.1:c.1023C>A XP_011534522.1:p.Cys341Ter
XM_011536221.1:c.*427C>A XP_011534523.1:n.*427C>A
XM_011536223.1:c.441C>A XP_011534525.1:p.Cys147Ter
XM_011536223.3:c.441C>A XP_011534525.1:p.Cys147Ter
XR_001743705.1:n.1625C>A
NM_003880.4:c.1023C>A NP_003871.1:p.Cys341Ter
NM_198239.2:c.1023C>A MANE Select NP_937882.2:p.Cys341Ter
NR_125353.2:n.1341C>A
NR_125354.3:n.1168C>A