Canonical Allele Identifier: CA365376434

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390722G>T (hg19) ; chr6:g.112069519G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069519G>T , CM000668.2:g.112069519G>T	GRCh38
NC_000006.11:g.112390722G>T , CM000668.1:g.112390722G>T	GRCh37
NC_000006.10:g.112497415G>T	NCBI36
NG_011748.1:g.20445G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.964G>T MANE Select	ENSP00000357655.4:p.Glu322Ter
ENST00000639360.1:c.865G>T	ENSP00000491774.1:p.Glu289Ter
ENST00000230529.9:c.964G>T	ENSP00000230529.5:p.Glu322Ter
ENST00000361714.5:c.964G>T	ENSP00000354734.2:p.Glu322Ter
ENST00000368663.4:c.*270G>T	ENSP00000357652.4:n.*270G>T
ENST00000368664.7:c.*368G>T	ENSP00000357653.3:n.*368G>T
ENST00000368666.6:c.1018G>T	ENSP00000357655.3:p.Glu340Ter
ENST00000409166.5:c.292G>T	ENSP00000386467.1:p.Glu98Ter
ENST00000454589.5:c.*368G>T	ENSP00000395928.1:n.*368G>T
ENST00000604763.5:c.964G>T	ENSP00000473777.1:p.Glu322Ter
ENST00000613648.1:n.799G>T
ENST00000620524.3:n.895G>T
NM_003880.3:c.964G>T	NP_003871.1:p.Glu322Ter
NM_198239.1:c.1018G>T	NP_937882.1:p.Glu340Ter
NR_125353.1:n.1218G>T
NR_125354.1:n.1138G>T
XM_011536220.1:c.964G>T	XP_011534522.1:p.Glu322Ter
XM_011536221.1:c.*368G>T	XP_011534523.1:n.*368G>T
XM_011536223.1:c.382G>T	XP_011534525.1:p.Glu128Ter
XM_011536223.3:c.382G>T	XP_011534525.1:p.Glu128Ter
XR_001743705.1:n.1566G>T
NM_003880.4:c.964G>T	NP_003871.1:p.Glu322Ter
NM_198239.2:c.964G>T MANE Select	NP_937882.2:p.Glu322Ter
NR_125353.2:n.1282G>T
NR_125354.3:n.1109G>T