Canonical Allele Identifier: CA451901405

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390727G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069524G>A , CM000668.2:g.112069524G>A	GRCh38
NC_000006.11:g.112390727G>A , CM000668.1:g.112390727G>A	GRCh37
NC_000006.10:g.112497420G>A	NCBI36
NG_011748.1:g.20450G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.969G>A MANE Select	ENSP00000357655.4:p.Gly323=
ENST00000639360.1:c.870G>A	ENSP00000491774.1:p.Gly290=
ENST00000230529.9:c.969G>A	ENSP00000230529.5:p.Gly323=
ENST00000361714.5:c.969G>A	ENSP00000354734.2:p.Gly323=
ENST00000368663.4:c.*275G>A	ENSP00000357652.4:n.*275G>A
ENST00000368664.7:c.*373G>A	ENSP00000357653.3:n.*373G>A
ENST00000368666.6:c.1023G>A	ENSP00000357655.3:p.Gly341=
ENST00000409166.5:c.297G>A	ENSP00000386467.1:p.Gly99=
ENST00000454589.5:c.*373G>A	ENSP00000395928.1:n.*373G>A
ENST00000604763.5:c.969G>A	ENSP00000473777.1:p.Gly323=
ENST00000613648.1:n.804G>A
ENST00000620524.3:n.900G>A
NM_003880.3:c.969G>A	NP_003871.1:p.Gly323=
NM_198239.1:c.1023G>A	NP_937882.1:p.Gly341=
NR_125353.1:n.1223G>A
NR_125354.1:n.1143G>A
XM_011536220.1:c.969G>A	XP_011534522.1:p.Gly323=
XM_011536221.1:c.*373G>A	XP_011534523.1:n.*373G>A
XM_011536223.1:c.387G>A	XP_011534525.1:p.Gly129=
XM_011536223.3:c.387G>A	XP_011534525.1:p.Gly129=
XR_001743705.1:n.1571G>A
NM_003880.4:c.969G>A	NP_003871.1:p.Gly323=
NM_198239.2:c.969G>A MANE Select	NP_937882.2:p.Gly323=
NR_125353.2:n.1287G>A
NR_125354.3:n.1114G>A