Canonical Allele Identifier: CA1655201589

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069548G= , CM000668.2:g.112069548G=	GRCh38
NC_000006.11:g.112390751G= , CM000668.1:g.112390751G=	GRCh37
NC_000006.10:g.112497444G=	NCBI36
NG_011748.1:g.20474G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.993G= MANE Select	ENSP00000357655.4:p.Trp331=
ENST00000639360.1:c.894G=	ENSP00000491774.1:p.Trp298=
ENST00000230529.9:c.993G=	ENSP00000230529.5:p.Trp331=
ENST00000361714.5:c.993G=	ENSP00000354734.2:p.Trp331=
ENST00000368663.4:c.*299G=	ENSP00000357652.4:n.*299G=
ENST00000368664.7:c.*397G=	ENSP00000357653.3:n.*397G=
ENST00000368666.6:c.1047G=	ENSP00000357655.3:p.Trp349=
ENST00000409166.5:c.321G=	ENSP00000386467.1:p.Trp107=
ENST00000454589.5:c.*397G=	ENSP00000395928.1:n.*397G=
ENST00000604763.5:c.993G=	ENSP00000473777.1:p.Trp331=
ENST00000613648.1:n.828G=
ENST00000620524.3:n.924G=
NM_003880.3:c.993G=	NP_003871.1:p.Trp331=
NM_198239.1:c.1047G=	NP_937882.1:p.Trp349=
NR_125353.1:n.1247G=
NR_125354.1:n.1167G=
XM_011536220.1:c.993G=	XP_011534522.1:p.Trp331=
XM_011536221.1:c.*397G=	XP_011534523.1:n.*397G=
XM_011536223.1:c.411G=	XP_011534525.1:p.Trp137=
XM_011536223.3:c.411G=	XP_011534525.1:p.Trp137=
XR_001743705.1:n.1595G=
NM_003880.4:c.993G=	NP_003871.1:p.Trp331=
NM_198239.2:c.993G= MANE Select	NP_937882.2:p.Trp331=
NR_125353.2:n.1311G=
NR_125354.3:n.1138G=