Canonical Allele Identifier: CA365376052

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390638A>C (hg19) ; chr6:g.112069435A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069435A>C , CM000668.2:g.112069435A>C	GRCh38
NC_000006.11:g.112390638A>C , CM000668.1:g.112390638A>C	GRCh37
NC_000006.10:g.112497331A>C	NCBI36
NG_011748.1:g.20361A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.880A>C MANE Select	ENSP00000357655.4:p.Thr294Pro
ENST00000639360.1:c.781A>C	ENSP00000491774.1:p.Thr261Pro
ENST00000230529.9:c.880A>C	ENSP00000230529.5:p.Thr294Pro
ENST00000361714.5:c.880A>C	ENSP00000354734.2:p.Thr294Pro
ENST00000368663.4:c.*186A>C	ENSP00000357652.4:n.*186A>C
ENST00000368664.7:c.*284A>C	ENSP00000357653.3:n.*284A>C
ENST00000368666.6:c.934A>C	ENSP00000357655.3:p.Thr312Pro
ENST00000409166.5:c.208A>C	ENSP00000386467.1:p.Thr70Pro
ENST00000454589.5:c.*284A>C	ENSP00000395928.1:n.*284A>C
ENST00000604763.5:c.880A>C	ENSP00000473777.1:p.Thr294Pro
ENST00000613648.1:n.715A>C
ENST00000620524.3:n.811A>C
NM_003880.3:c.880A>C	NP_003871.1:p.Thr294Pro
NM_198239.1:c.934A>C	NP_937882.1:p.Thr312Pro
NR_125353.1:n.1134A>C
NR_125354.1:n.1054A>C
XM_011536220.1:c.880A>C	XP_011534522.1:p.Thr294Pro
XM_011536221.1:c.*284A>C	XP_011534523.1:n.*284A>C
XM_011536223.1:c.298A>C	XP_011534525.1:p.Thr100Pro
XM_011536223.3:c.298A>C	XP_011534525.1:p.Thr100Pro
XR_001743705.1:n.1482A>C
NM_003880.4:c.880A>C	NP_003871.1:p.Thr294Pro
NM_198239.2:c.880A>C MANE Select	NP_937882.2:p.Thr294Pro
NR_125353.2:n.1198A>C
NR_125354.3:n.1025A>C