Canonical Allele Identifier: CA365369522

Gene: CCN6

Linked Data

• COSMIC: COSM1439860
• MyVariant Identifiers: chr6:g.112382397A>C (hg19) ; chr6:g.112061194A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061194A>C , CM000668.2:g.112061194A>C	GRCh38
NC_000006.11:g.112382397A>C , CM000668.1:g.112382397A>C	GRCh37
NC_000006.10:g.112489090A>C	NCBI36
NG_011748.1:g.12120A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.252A>C MANE Select	ENSP00000357655.4:p.Glu84Asp
ENST00000639360.1:c.156A>C	ENSP00000491774.1:p.Glu52Asp
ENST00000230529.9:c.252A>C	ENSP00000230529.5:p.Glu84Asp
ENST00000361714.5:c.252A>C	ENSP00000354734.2:p.Glu84Asp
ENST00000368663.4:c.252A>C	ENSP00000357652.4:p.Glu84Asp
ENST00000368664.7:c.306A>C	ENSP00000357653.3:p.Glu102Asp
ENST00000368666.6:c.306A>C	ENSP00000357655.3:p.Glu102Asp
ENST00000409166.5:c.-507-85A>C	ENSP00000386467.1:n.-507-85A>C
ENST00000454589.5:c.252A>C	ENSP00000395928.1:p.Glu84Asp
ENST00000604763.5:c.252A>C	ENSP00000473777.1:p.Glu84Asp
ENST00000620524.3:n.186A>C
NM_003880.3:c.252A>C	NP_003871.1:p.Glu84Asp
NM_198239.1:c.306A>C	NP_937882.1:p.Glu102Asp
NR_125353.1:n.442A>C
NR_125354.1:n.362A>C
XM_011536220.1:c.252A>C	XP_011534522.1:p.Glu84Asp
XM_011536221.1:c.315A>C	XP_011534523.1:p.Glu105Asp
XM_011536222.1:c.390A>C	XP_011534524.1:p.Glu130Asp
XM_011536222.2:c.315A>C	XP_011534524.2:p.Glu105Asp
XR_001743705.1:n.790A>C
NM_003880.4:c.252A>C	NP_003871.1:p.Glu84Asp
NM_198239.2:c.252A>C MANE Select	NP_937882.2:p.Glu84Asp
NR_125353.2:n.506A>C
NR_125354.3:n.333A>C