Canonical Allele Identifier: CA365376742

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390764G>A (hg19) ; chr6:g.112069561G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069561G>A , CM000668.2:g.112069561G>A	GRCh38
NC_000006.11:g.112390764G>A , CM000668.1:g.112390764G>A	GRCh37
NC_000006.10:g.112497457G>A	NCBI36
NG_011748.1:g.20487G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1006G>A MANE Select	ENSP00000357655.4:p.Val336Met
ENST00000639360.1:c.907G>A	ENSP00000491774.1:p.Val303Met
ENST00000230529.9:c.1006G>A	ENSP00000230529.5:p.Val336Met
ENST00000361714.5:c.1006G>A	ENSP00000354734.2:p.Val336Met
ENST00000368663.4:c.*312G>A	ENSP00000357652.4:n.*312G>A
ENST00000368664.7:c.*410G>A	ENSP00000357653.3:n.*410G>A
ENST00000368666.6:c.1060G>A	ENSP00000357655.3:p.Val354Met
ENST00000409166.5:c.334G>A	ENSP00000386467.1:p.Val112Met
ENST00000454589.5:c.*410G>A	ENSP00000395928.1:n.*410G>A
ENST00000604763.5:c.1006G>A	ENSP00000473777.1:p.Val336Met
ENST00000613648.1:n.841G>A
ENST00000620524.3:n.937G>A
NM_003880.3:c.1006G>A	NP_003871.1:p.Val336Met
NM_198239.1:c.1060G>A	NP_937882.1:p.Val354Met
NR_125353.1:n.1260G>A
NR_125354.1:n.1180G>A
XM_011536220.1:c.1006G>A	XP_011534522.1:p.Val336Met
XM_011536221.1:c.*410G>A	XP_011534523.1:n.*410G>A
XM_011536223.1:c.424G>A	XP_011534525.1:p.Val142Met
XM_011536223.3:c.424G>A	XP_011534525.1:p.Val142Met
XR_001743705.1:n.1608G>A
NM_003880.4:c.1006G>A	NP_003871.1:p.Val336Met
NM_198239.2:c.1006G>A MANE Select	NP_937882.2:p.Val336Met
NR_125353.2:n.1324G>A
NR_125354.3:n.1151G>A