Canonical Allele Identifier: CA365376607

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390746C>G (hg19) ; chr6:g.112069543C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069543C>G , CM000668.2:g.112069543C>G	GRCh38
NC_000006.11:g.112390746C>G , CM000668.1:g.112390746C>G	GRCh37
NC_000006.10:g.112497439C>G	NCBI36
NG_011748.1:g.20469C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.988C>G MANE Select	ENSP00000357655.4:p.Leu330Val
ENST00000639360.1:c.889C>G	ENSP00000491774.1:p.Leu297Val
ENST00000230529.9:c.988C>G	ENSP00000230529.5:p.Leu330Val
ENST00000361714.5:c.988C>G	ENSP00000354734.2:p.Leu330Val
ENST00000368663.4:c.*294C>G	ENSP00000357652.4:n.*294C>G
ENST00000368664.7:c.*392C>G	ENSP00000357653.3:n.*392C>G
ENST00000368666.6:c.1042C>G	ENSP00000357655.3:p.Leu348Val
ENST00000409166.5:c.316C>G	ENSP00000386467.1:p.Leu106Val
ENST00000454589.5:c.*392C>G	ENSP00000395928.1:n.*392C>G
ENST00000604763.5:c.988C>G	ENSP00000473777.1:p.Leu330Val
ENST00000613648.1:n.823C>G
ENST00000620524.3:n.919C>G
NM_003880.3:c.988C>G	NP_003871.1:p.Leu330Val
NM_198239.1:c.1042C>G	NP_937882.1:p.Leu348Val
NR_125353.1:n.1242C>G
NR_125354.1:n.1162C>G
XM_011536220.1:c.988C>G	XP_011534522.1:p.Leu330Val
XM_011536221.1:c.*392C>G	XP_011534523.1:n.*392C>G
XM_011536223.1:c.406C>G	XP_011534525.1:p.Leu136Val
XM_011536223.3:c.406C>G	XP_011534525.1:p.Leu136Val
XR_001743705.1:n.1590C>G
NM_003880.4:c.988C>G	NP_003871.1:p.Leu330Val
NM_198239.2:c.988C>G MANE Select	NP_937882.2:p.Leu330Val
NR_125353.2:n.1306C>G
NR_125354.3:n.1133C>G