Canonical Allele Identifier: CA1655201555

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069439T= , CM000668.2:g.112069439T=	GRCh38
NC_000006.11:g.112390642T= , CM000668.1:g.112390642T=	GRCh37
NC_000006.10:g.112497335T=	NCBI36
NG_011748.1:g.20365T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.884T= MANE Select	ENSP00000357655.4:p.Phe295=
ENST00000639360.1:c.785T=	ENSP00000491774.1:p.Phe262=
ENST00000230529.9:c.884T=	ENSP00000230529.5:p.Phe295=
ENST00000361714.5:c.884T=	ENSP00000354734.2:p.Phe295=
ENST00000368663.4:c.*190T=	ENSP00000357652.4:n.*190T=
ENST00000368664.7:c.*288T=	ENSP00000357653.3:n.*288T=
ENST00000368666.6:c.938T=	ENSP00000357655.3:p.Phe313=
ENST00000409166.5:c.212T=	ENSP00000386467.1:p.Phe71=
ENST00000454589.5:c.*288T=	ENSP00000395928.1:n.*288T=
ENST00000604763.5:c.884T=	ENSP00000473777.1:p.Phe295=
ENST00000613648.1:n.719T=
ENST00000620524.3:n.815T=
NM_003880.3:c.884T=	NP_003871.1:p.Phe295=
NM_198239.1:c.938T=	NP_937882.1:p.Phe313=
NR_125353.1:n.1138T=
NR_125354.1:n.1058T=
XM_011536220.1:c.884T=	XP_011534522.1:p.Phe295=
XM_011536221.1:c.*288T=	XP_011534523.1:n.*288T=
XM_011536223.1:c.302T=	XP_011534525.1:p.Phe101=
XM_011536223.3:c.302T=	XP_011534525.1:p.Phe101=
XR_001743705.1:n.1486T=
NM_003880.4:c.884T=	NP_003871.1:p.Phe295=
NM_198239.2:c.884T= MANE Select	NP_937882.2:p.Phe295=
NR_125353.2:n.1202T=
NR_125354.3:n.1029T=