Canonical Allele Identifier: CA365369434
Gene: CCN6 HGNC NCBI

Linked Data

COSMIC: COSM739612

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112061182G>T , CM000668.2:g.112061182G>T GRCh38
NC_000006.11:g.112382385G>T , CM000668.1:g.112382385G>T GRCh37
NC_000006.10:g.112489078G>T NCBI36
NG_011748.1:g.12108G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000368666.7:c.240G>T MANE Select ENSP00000357655.4:p.Lys80Asn
ENST00000639360.1:c.144G>T ENSP00000491774.1:p.Lys48Asn
ENST00000230529.9:c.240G>T ENSP00000230529.5:p.Lys80Asn
ENST00000361714.5:c.240G>T ENSP00000354734.2:p.Lys80Asn
ENST00000368663.4:c.240G>T ENSP00000357652.4:p.Lys80Asn
ENST00000368664.7:c.294G>T ENSP00000357653.3:p.Lys98Asn
ENST00000368666.6:c.294G>T ENSP00000357655.3:p.Lys98Asn
ENST00000409166.5:c.-507-97G>T ENSP00000386467.1:n.-507-97G>T
ENST00000454589.5:c.240G>T ENSP00000395928.1:p.Lys80Asn
ENST00000604763.5:c.240G>T ENSP00000473777.1:p.Lys80Asn
ENST00000620524.3:n.174G>T
NM_003880.3:c.240G>T NP_003871.1:p.Lys80Asn
NM_198239.1:c.294G>T NP_937882.1:p.Lys98Asn
NR_125353.1:n.430G>T
NR_125354.1:n.350G>T
XM_011536220.1:c.240G>T XP_011534522.1:p.Lys80Asn
XM_011536221.1:c.303G>T XP_011534523.1:p.Lys101Asn
XM_011536222.1:c.378G>T XP_011534524.1:p.Lys126Asn
XM_011536222.2:c.303G>T XP_011534524.2:p.Lys101Asn
XR_001743705.1:n.778G>T
NM_003880.4:c.240G>T NP_003871.1:p.Lys80Asn
NM_198239.2:c.240G>T MANE Select NP_937882.2:p.Lys80Asn
NR_125353.2:n.494G>T
NR_125354.3:n.321G>T