Canonical Allele Identifier: CA365376138

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069451-G-A
• MyVariant Identifiers: chr6:g.112390654G>A (hg19) ; chr6:g.112069451G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069451G>A , CM000668.2:g.112069451G>A	GRCh38
NC_000006.11:g.112390654G>A , CM000668.1:g.112390654G>A	GRCh37
NC_000006.10:g.112497347G>A	NCBI36
NG_011748.1:g.20377G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.896G>A MANE Select	ENSP00000357655.4:p.Cys299Tyr
ENST00000639360.1:c.797G>A	ENSP00000491774.1:p.Cys266Tyr
ENST00000230529.9:c.896G>A	ENSP00000230529.5:p.Cys299Tyr
ENST00000361714.5:c.896G>A	ENSP00000354734.2:p.Cys299Tyr
ENST00000368663.4:c.*202G>A	ENSP00000357652.4:n.*202G>A
ENST00000368664.7:c.*300G>A	ENSP00000357653.3:n.*300G>A
ENST00000368666.6:c.950G>A	ENSP00000357655.3:p.Cys317Tyr
ENST00000409166.5:c.224G>A	ENSP00000386467.1:p.Cys75Tyr
ENST00000454589.5:c.*300G>A	ENSP00000395928.1:n.*300G>A
ENST00000604763.5:c.896G>A	ENSP00000473777.1:p.Cys299Tyr
ENST00000613648.1:n.731G>A
ENST00000620524.3:n.827G>A
NM_003880.3:c.896G>A	NP_003871.1:p.Cys299Tyr
NM_198239.1:c.950G>A	NP_937882.1:p.Cys317Tyr
NR_125353.1:n.1150G>A
NR_125354.1:n.1070G>A
XM_011536220.1:c.896G>A	XP_011534522.1:p.Cys299Tyr
XM_011536221.1:c.*300G>A	XP_011534523.1:n.*300G>A
XM_011536223.1:c.314G>A	XP_011534525.1:p.Cys105Tyr
XM_011536223.3:c.314G>A	XP_011534525.1:p.Cys105Tyr
XR_001743705.1:n.1498G>A
NM_003880.4:c.896G>A	NP_003871.1:p.Cys299Tyr
NM_198239.2:c.896G>A MANE Select	NP_937882.2:p.Cys299Tyr
NR_125353.2:n.1214G>A
NR_125354.3:n.1041G>A