Canonical Allele Identifier: CA278864
Gene: CCN6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069417_112069418dup , CM000668.2:g.112069417_112069418dup GRCh38
NC_000006.11:g.112390620_112390621dup , CM000668.1:g.112390620_112390621dup GRCh37
NC_000006.10:g.112497313_112497314dup NCBI36
NG_011748.1:g.20343_20344dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000368666.7:c.862_863dup MANE Select ENSP00000357655.4:p.Gln289LeufsTer25
ENST00000639360.1:c.763_764dup ENSP00000491774.1:p.Gln256LeufsTer25
ENST00000230529.9:c.862_863dup ENSP00000230529.5:p.Gln289LeufsTer25
ENST00000361714.5:c.862_863dup ENSP00000354734.2:p.Gln289LeufsTer25
ENST00000368663.4:c.*168_*169dup ENSP00000357652.4:n.*168_*169dup
ENST00000368664.7:c.*266_*267dup ENSP00000357653.3:n.*266_*267dup
ENST00000368666.6:c.916_917dup ENSP00000357655.3:p.Gln307LeufsTer25
ENST00000409166.5:c.190_191dup ENSP00000386467.1:p.Gln65LeufsTer25
ENST00000454589.5:c.*266_*267dup ENSP00000395928.1:n.*266_*267dup
ENST00000604763.5:c.862_863dup ENSP00000473777.1:p.Gln289LeufsTer25
ENST00000613648.1:n.697_698dup
ENST00000620524.3:n.793_794dup
NM_003880.3:c.862_863dup NP_003871.1:p.Gln289LeufsTer25
NM_198239.1:c.916_917dup NP_937882.1:p.Gln307LeufsTer25
NR_125353.1:n.1116_1117dup
NR_125354.1:n.1036_1037dup
XM_011536220.1:c.862_863dup XP_011534522.1:p.Gln289LeufsTer25
XM_011536221.1:c.*266_*267dup XP_011534523.1:n.*266_*267dup
XM_011536223.1:c.280_281dup XP_011534525.1:p.Gln95LeufsTer25
XM_011536223.3:c.280_281dup XP_011534525.1:p.Gln95LeufsTer25
XR_001743705.1:n.1464_1465dup
NM_003880.4:c.862_863dup NP_003871.1:p.Gln289LeufsTer25
NM_198239.2:c.862_863dup MANE Select NP_937882.2:p.Gln289LeufsTer25
NR_125353.2:n.1180_1181dup
NR_125354.3:n.1007_1008dup
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Search 100 bp 3'