Canonical Allele Identifier: CA3135080694

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112054407T= , CM000668.2:g.112054407T=	GRCh38
NC_000006.11:g.112375610T= , CM000668.1:g.112375610T=	GRCh37
NC_000006.10:g.112482303T=	NCBI36
NG_011748.1:g.5333T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.48+2T= MANE Select	ENSP00000357655.4:n.48+2T=
ENST00000674325.1:c.48+2T=	ENSP00000501404.1:n.48+2T=
ENST00000230529.9:c.48+2T=	ENSP00000230529.5:n.48+2T=
ENST00000361714.5:c.48+2T=	ENSP00000354734.2:n.48+2T=
ENST00000368663.4:c.48+2T=	ENSP00000357652.4:n.48+2T=
ENST00000368664.7:c.102+2T=	ENSP00000357653.3:n.102+2T=
ENST00000368666.6:c.102+2T=	ENSP00000357655.3:n.102+2T=
ENST00000409166.5:c.-508+173T=	ENSP00000386467.1:n.-508+173T=
ENST00000454589.5:c.48+2T=	ENSP00000395928.1:n.48+2T=
ENST00000483439.1:n.222+2T=
ENST00000604763.5:c.48+2T=	ENSP00000473777.1:n.48+2T=
NM_003880.3:c.48+2T=	NP_003871.1:n.48+2T=
NM_198239.1:c.102+2T=	NP_937882.1:n.102+2T=
NR_125353.1:n.238+2T=
NR_125354.1:n.158+2T=
XM_011536220.1:c.48+2T=	XP_011534522.1:n.48+2T=
XM_011536221.1:c.111+2T=	XP_011534523.1:n.111+2T=
XM_011536222.1:c.186+2T=	XP_011534524.1:n.186+2T=
XM_011536222.2:c.111+2T=	XP_011534524.2:n.111+2T=
XR_001743705.1:n.586+2T=
NM_003880.4:c.48+2T=	NP_003871.1:n.48+2T=
NM_198239.2:c.48+2T= MANE Select	NP_937882.2:n.48+2T=
NR_125353.2:n.302+2T=
NR_125354.3:n.129+2T=