Canonical Allele Identifier: CA365376146

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069452C>A , CM000668.2:g.112069452C>A	GRCh38
NC_000006.11:g.112390655C>A , CM000668.1:g.112390655C>A	GRCh37
NC_000006.10:g.112497348C>A	NCBI36
NG_011748.1:g.20378C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_198239.2:c.897C>A MANE Select	NP_937882.2:p.Cys299Ter
ENST00000368666.7:c.897C>A MANE Select	ENSP00000357655.4:p.Cys299Ter
NM_003880.3:c.897C>A	NP_003871.1:p.Cys299Ter
NM_003880.4:c.897C>A	NP_003871.1:p.Cys299Ter
NM_198239.1:c.951C>A	NP_937882.1:p.Cys317Ter
NR_125353.1:n.1151C>A
NR_125353.2:n.1215C>A
NR_125354.1:n.1071C>A
NR_125354.3:n.1042C>A
ENST00000230529.9:c.897C>A	ENSP00000230529.5:p.Cys299Ter
ENST00000361714.5:c.897C>A	ENSP00000354734.2:p.Cys299Ter
ENST00000368663.4:c.*203C>A	ENSP00000357652.4:n.*203C>A
ENST00000368664.7:c.*301C>A	ENSP00000357653.3:n.*301C>A
ENST00000368666.6:c.951C>A	ENSP00000357655.3:p.Cys317Ter
ENST00000409166.5:c.225C>A	ENSP00000386467.1:p.Cys75Ter
ENST00000454589.5:c.*301C>A	ENSP00000395928.1:n.*301C>A
ENST00000604763.5:c.897C>A	ENSP00000473777.1:p.Cys299Ter
ENST00000613648.1:n.732C>A
ENST00000620524.3:n.828C>A
ENST00000639360.1:c.798C>A	ENSP00000491774.1:p.Cys266Ter
XM_011536220.1:c.897C>A	XP_011534522.1:p.Cys299Ter
XM_011536221.1:c.*301C>A	XP_011534523.1:n.*301C>A
XM_011536223.1:c.315C>A	XP_011534525.1:p.Cys105Ter
XM_011536223.3:c.315C>A	XP_011534525.1:p.Cys105Ter
XR_001743705.1:n.1499C>A