Canonical Allele Identifier: CA1655201600

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069574A= , CM000668.2:g.112069574A=	GRCh38
NC_000006.11:g.112390777A= , CM000668.1:g.112390777A=	GRCh37
NC_000006.10:g.112497470A=	NCBI36
NG_011748.1:g.20500A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1019A= MANE Select	ENSP00000357655.4:p.Asn340=
ENST00000639360.1:c.920A=	ENSP00000491774.1:p.Asn307=
ENST00000230529.9:c.1019A=	ENSP00000230529.5:p.Asn340=
ENST00000361714.5:c.1019A=	ENSP00000354734.2:p.Asn340=
ENST00000368663.4:c.*325A=	ENSP00000357652.4:n.*325A=
ENST00000368664.7:c.*423A=	ENSP00000357653.3:n.*423A=
ENST00000368666.6:c.1073A=	ENSP00000357655.3:p.Asn358=
ENST00000409166.5:c.347A=	ENSP00000386467.1:p.Asn116=
ENST00000454589.5:c.*423A=	ENSP00000395928.1:n.*423A=
ENST00000604763.5:c.1019A=	ENSP00000473777.1:p.Asn340=
ENST00000613648.1:n.854A=
ENST00000620524.3:n.950A=
NM_003880.3:c.1019A=	NP_003871.1:p.Asn340=
NM_198239.1:c.1073A=	NP_937882.1:p.Asn358=
NR_125353.1:n.1273A=
NR_125354.1:n.1193A=
XM_011536220.1:c.1019A=	XP_011534522.1:p.Asn340=
XM_011536221.1:c.*423A=	XP_011534523.1:n.*423A=
XM_011536223.1:c.437A=	XP_011534525.1:p.Asn146=
XM_011536223.3:c.437A=	XP_011534525.1:p.Asn146=
XR_001743705.1:n.1621A=
NM_003880.4:c.1019A=	NP_003871.1:p.Asn340=
NM_198239.2:c.1019A= MANE Select	NP_937882.2:p.Asn340=
NR_125353.2:n.1337A=
NR_125354.3:n.1164A=