Canonical Allele Identifier: CA1655199539

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112064842G= , CM000668.2:g.112064842G=	GRCh38
NC_000006.11:g.112386045G= , CM000668.1:g.112386045G=	GRCh37
NC_000006.10:g.112492738G=	NCBI36
NG_011748.1:g.15768G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.434G= MANE Select	ENSP00000357655.4:p.Cys145=
ENST00000639360.1:c.335G=	ENSP00000491774.1:p.Cys112=
ENST00000230529.9:c.434G=	ENSP00000230529.5:p.Cys145=
ENST00000361714.5:c.434G=	ENSP00000354734.2:p.Cys145=
ENST00000368663.4:c.434G=	ENSP00000357652.4:p.Cys145=
ENST00000368664.7:c.488G=	ENSP00000357653.3:p.Cys163=
ENST00000368666.6:c.488G=	ENSP00000357655.3:p.Cys163=
ENST00000409166.5:c.-303G=	ENSP00000386467.1:n.-303G=
ENST00000454589.5:c.434G=	ENSP00000395928.1:p.Cys145=
ENST00000604763.5:c.434G=	ENSP00000473777.1:p.Cys145=
ENST00000613648.1:n.205G=
ENST00000620524.3:n.365G=
NM_003880.3:c.434G=	NP_003871.1:p.Cys145=
NM_198239.1:c.488G=	NP_937882.1:p.Cys163=
NR_125353.1:n.624G=
NR_125354.1:n.544G=
XM_011536220.1:c.434G=	XP_011534522.1:p.Cys145=
XM_011536221.1:c.497G=	XP_011534523.1:p.Cys166=
XM_011536222.1:c.516+56G=	XP_011534524.1:n.516+56G=
XM_011536223.1:c.-149G=	XP_011534525.1:n.-149G=
XM_011536222.2:c.441+56G=	XP_011534524.2:n.441+56G=
XM_011536223.3:c.-149G=	XP_011534525.1:n.-149G=
XR_001743705.1:n.972G=
NM_003880.4:c.434G=	NP_003871.1:p.Cys145=
NM_198239.2:c.434G= MANE Select	NP_937882.2:p.Cys145=
NR_125353.2:n.688G=
NR_125354.3:n.515G=