Canonical Allele Identifier: CA451598855

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390808G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069605G>A , CM000668.2:g.112069605G>A	GRCh38
NC_000006.11:g.112390808G>A , CM000668.1:g.112390808G>A	GRCh37
NC_000006.10:g.112497501G>A	NCBI36
NG_011748.1:g.20531G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1050G>A MANE Select	ENSP00000357655.4:p.Glu350=
ENST00000639360.1:c.951G>A	ENSP00000491774.1:p.Glu317=
ENST00000230529.9:c.1050G>A	ENSP00000230529.5:p.Glu350=
ENST00000361714.5:c.1050G>A	ENSP00000354734.2:p.Glu350=
ENST00000368663.4:c.*356G>A	ENSP00000357652.4:n.*356G>A
ENST00000368664.7:c.*454G>A	ENSP00000357653.3:n.*454G>A
ENST00000368666.6:c.1104G>A	ENSP00000357655.3:p.Glu368=
ENST00000409166.5:c.378G>A	ENSP00000386467.1:p.Glu126=
ENST00000454589.5:c.*454G>A	ENSP00000395928.1:n.*454G>A
ENST00000604763.5:c.1050G>A	ENSP00000473777.1:p.Glu350=
ENST00000613648.1:n.885G>A
ENST00000620524.3:n.981G>A
NM_003880.3:c.1050G>A	NP_003871.1:p.Glu350=
NM_198239.1:c.1104G>A	NP_937882.1:p.Glu368=
NR_125353.1:n.1304G>A
NR_125354.1:n.1224G>A
XM_011536220.1:c.1050G>A	XP_011534522.1:p.Glu350=
XM_011536221.1:c.*454G>A	XP_011534523.1:n.*454G>A
XM_011536223.1:c.468G>A	XP_011534525.1:p.Glu156=
XM_011536223.3:c.468G>A	XP_011534525.1:p.Glu156=
XR_001743705.1:n.1652G>A
NM_003880.4:c.1050G>A	NP_003871.1:p.Glu350=
NM_198239.2:c.1050G>A MANE Select	NP_937882.2:p.Glu350=
NR_125353.2:n.1368G>A
NR_125354.3:n.1195G>A