Canonical Allele Identifier: CA365377056

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390809C>G (hg19) ; chr6:g.112069606C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069606C>G , CM000668.2:g.112069606C>G	GRCh38
NC_000006.11:g.112390809C>G , CM000668.1:g.112390809C>G	GRCh37
NC_000006.10:g.112497502C>G	NCBI36
NG_011748.1:g.20532C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1051C>G MANE Select	ENSP00000357655.4:p.Leu351Val
ENST00000639360.1:c.952C>G	ENSP00000491774.1:p.Leu318Val
ENST00000230529.9:c.1051C>G	ENSP00000230529.5:p.Leu351Val
ENST00000361714.5:c.1051C>G	ENSP00000354734.2:p.Leu351Val
ENST00000368663.4:c.*357C>G	ENSP00000357652.4:n.*357C>G
ENST00000368664.7:c.*455C>G	ENSP00000357653.3:n.*455C>G
ENST00000368666.6:c.1105C>G	ENSP00000357655.3:p.Leu369Val
ENST00000409166.5:c.379C>G	ENSP00000386467.1:p.Leu127Val
ENST00000454589.5:c.*455C>G	ENSP00000395928.1:n.*455C>G
ENST00000604763.5:c.1051C>G	ENSP00000473777.1:p.Leu351Val
ENST00000613648.1:n.886C>G
ENST00000620524.3:n.982C>G
NM_003880.3:c.1051C>G	NP_003871.1:p.Leu351Val
NM_198239.1:c.1105C>G	NP_937882.1:p.Leu369Val
NR_125353.1:n.1305C>G
NR_125354.1:n.1225C>G
XM_011536220.1:c.1051C>G	XP_011534522.1:p.Leu351Val
XM_011536221.1:c.*455C>G	XP_011534523.1:n.*455C>G
XM_011536223.1:c.469C>G	XP_011534525.1:p.Leu157Val
XM_011536223.3:c.469C>G	XP_011534525.1:p.Leu157Val
XR_001743705.1:n.1653C>G
NM_003880.4:c.1051C>G	NP_003871.1:p.Leu351Val
NM_198239.2:c.1051C>G MANE Select	NP_937882.2:p.Leu351Val
NR_125353.2:n.1369C>G
NR_125354.3:n.1196C>G