Canonical Allele Identifier: CA365367713

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382201G>A (hg19) ; chr6:g.112060998G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112060998G>A , CM000668.2:g.112060998G>A	GRCh38
NC_000006.11:g.112382201G>A , CM000668.1:g.112382201G>A	GRCh37
NC_000006.10:g.112488894G>A	NCBI36
NG_011748.1:g.11924G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.56G>A MANE Select	ENSP00000357655.4:p.Cys19Tyr
ENST00000230529.9:c.56G>A	ENSP00000230529.5:p.Cys19Tyr
ENST00000361714.5:c.56G>A	ENSP00000354734.2:p.Cys19Tyr
ENST00000368663.4:c.56G>A	ENSP00000357652.4:p.Cys19Tyr
ENST00000368664.7:c.110G>A	ENSP00000357653.3:p.Cys37Tyr
ENST00000368666.6:c.110G>A	ENSP00000357655.3:p.Cys37Tyr
ENST00000409166.5:c.-507-281G>A	ENSP00000386467.1:n.-507-281G>A
ENST00000454589.5:c.56G>A	ENSP00000395928.1:p.Cys19Tyr
ENST00000604763.5:c.56G>A	ENSP00000473777.1:p.Cys19Tyr
ENST00000620524.3:n.64-74G>A
NM_003880.3:c.56G>A	NP_003871.1:p.Cys19Tyr
NM_198239.1:c.110G>A	NP_937882.1:p.Cys37Tyr
NR_125353.1:n.246G>A
NR_125354.1:n.166G>A
XM_011536220.1:c.56G>A	XP_011534522.1:p.Cys19Tyr
XM_011536221.1:c.119G>A	XP_011534523.1:p.Cys40Tyr
XM_011536222.1:c.194G>A	XP_011534524.1:p.Cys65Tyr
XM_011536222.2:c.119G>A	XP_011534524.2:p.Cys40Tyr
XR_001743705.1:n.594G>A
NM_003880.4:c.56G>A	NP_003871.1:p.Cys19Tyr
NM_198239.2:c.56G>A MANE Select	NP_937882.2:p.Cys19Tyr
NR_125353.2:n.310G>A
NR_125354.3:n.137G>A