Canonical Allele Identifier: CA365376165

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390659G>T (hg19) ; chr6:g.112069456G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069456G>T , CM000668.2:g.112069456G>T	GRCh38
NC_000006.11:g.112390659G>T , CM000668.1:g.112390659G>T	GRCh37
NC_000006.10:g.112497352G>T	NCBI36
NG_011748.1:g.20382G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.901G>T MANE Select	ENSP00000357655.4:p.Asp301Tyr
ENST00000639360.1:c.802G>T	ENSP00000491774.1:p.Asp268Tyr
ENST00000230529.9:c.901G>T	ENSP00000230529.5:p.Asp301Tyr
ENST00000361714.5:c.901G>T	ENSP00000354734.2:p.Asp301Tyr
ENST00000368663.4:c.*207G>T	ENSP00000357652.4:n.*207G>T
ENST00000368664.7:c.*305G>T	ENSP00000357653.3:n.*305G>T
ENST00000368666.6:c.955G>T	ENSP00000357655.3:p.Asp319Tyr
ENST00000409166.5:c.229G>T	ENSP00000386467.1:p.Asp77Tyr
ENST00000454589.5:c.*305G>T	ENSP00000395928.1:n.*305G>T
ENST00000604763.5:c.901G>T	ENSP00000473777.1:p.Asp301Tyr
ENST00000613648.1:n.736G>T
ENST00000620524.3:n.832G>T
NM_003880.3:c.901G>T	NP_003871.1:p.Asp301Tyr
NM_198239.1:c.955G>T	NP_937882.1:p.Asp319Tyr
NR_125353.1:n.1155G>T
NR_125354.1:n.1075G>T
XM_011536220.1:c.901G>T	XP_011534522.1:p.Asp301Tyr
XM_011536221.1:c.*305G>T	XP_011534523.1:n.*305G>T
XM_011536223.1:c.319G>T	XP_011534525.1:p.Asp107Tyr
XM_011536223.3:c.319G>T	XP_011534525.1:p.Asp107Tyr
XR_001743705.1:n.1503G>T
NM_003880.4:c.901G>T	NP_003871.1:p.Asp301Tyr
NM_198239.2:c.901G>T MANE Select	NP_937882.2:p.Asp301Tyr
NR_125353.2:n.1219G>T
NR_125354.3:n.1046G>T