Canonical Allele Identifier: CA1655198621
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112061071G= , CM000668.2:g.112061071G= GRCh38
NC_000006.11:g.112382274G= , CM000668.1:g.112382274G= GRCh37
NC_000006.10:g.112488967G= NCBI36
NG_011748.1:g.11997G=

Transcript Alleles

HGVS Amino-acid change
ENST00000368666.7:c.129G= MANE Select ENSP00000357655.4:p.Gln43=
ENST00000639360.1:c.33G= ENSP00000491774.1:p.Gln11=
ENST00000230529.9:c.129G= ENSP00000230529.5:p.Gln43=
ENST00000361714.5:c.129G= ENSP00000354734.2:p.Gln43=
ENST00000368663.4:c.129G= ENSP00000357652.4:p.Gln43=
ENST00000368664.7:c.183G= ENSP00000357653.3:p.Gln61=
ENST00000368666.6:c.183G= ENSP00000357655.3:p.Gln61=
ENST00000409166.5:c.-507-208G= ENSP00000386467.1:n.-507-208G=
ENST00000454589.5:c.129G= ENSP00000395928.1:p.Gln43=
ENST00000604763.5:c.129G= ENSP00000473777.1:p.Gln43=
ENST00000620524.3:n.64-1G=
NM_003880.3:c.129G= NP_003871.1:p.Gln43=
NM_198239.1:c.183G= NP_937882.1:p.Gln61=
NR_125353.1:n.319G=
NR_125354.1:n.239G=
XM_011536220.1:c.129G= XP_011534522.1:p.Gln43=
XM_011536221.1:c.192G= XP_011534523.1:p.Gln64=
XM_011536222.1:c.267G= XP_011534524.1:p.Gln89=
XM_011536222.2:c.192G= XP_011534524.2:p.Gln64=
XR_001743705.1:n.667G=
NM_003880.4:c.129G= NP_003871.1:p.Gln43=
NM_198239.2:c.129G= MANE Select NP_937882.2:p.Gln43=
NR_125353.2:n.383G=
NR_125354.3:n.210G=