Canonical Allele Identifier: CA451598802

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390799A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069596A>T , CM000668.2:g.112069596A>T	GRCh38
NC_000006.11:g.112390799A>T , CM000668.1:g.112390799A>T	GRCh37
NC_000006.10:g.112497492A>T	NCBI36
NG_011748.1:g.20522A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1041A>T MANE Select	ENSP00000357655.4:p.Ile347=
ENST00000639360.1:c.942A>T	ENSP00000491774.1:p.Ile314=
ENST00000230529.9:c.1041A>T	ENSP00000230529.5:p.Ile347=
ENST00000361714.5:c.1041A>T	ENSP00000354734.2:p.Ile347=
ENST00000368663.4:c.*347A>T	ENSP00000357652.4:n.*347A>T
ENST00000368664.7:c.*445A>T	ENSP00000357653.3:n.*445A>T
ENST00000368666.6:c.1095A>T	ENSP00000357655.3:p.Ile365=
ENST00000409166.5:c.369A>T	ENSP00000386467.1:p.Ile123=
ENST00000454589.5:c.*445A>T	ENSP00000395928.1:n.*445A>T
ENST00000604763.5:c.1041A>T	ENSP00000473777.1:p.Ile347=
ENST00000613648.1:n.876A>T
ENST00000620524.3:n.972A>T
NM_003880.3:c.1041A>T	NP_003871.1:p.Ile347=
NM_198239.1:c.1095A>T	NP_937882.1:p.Ile365=
NR_125353.1:n.1295A>T
NR_125354.1:n.1215A>T
XM_011536220.1:c.1041A>T	XP_011534522.1:p.Ile347=
XM_011536221.1:c.*445A>T	XP_011534523.1:n.*445A>T
XM_011536223.1:c.459A>T	XP_011534525.1:p.Ile153=
XM_011536223.3:c.459A>T	XP_011534525.1:p.Ile153=
XR_001743705.1:n.1643A>T
NM_003880.4:c.1041A>T	NP_003871.1:p.Ile347=
NM_198239.2:c.1041A>T MANE Select	NP_937882.2:p.Ile347=
NR_125353.2:n.1359A>T
NR_125354.3:n.1186A>T