Canonical Allele Identifier: CA365376060

Gene: CCN6

Linked Data

• dbSNP Id: rs1336361698
• MyVariant Identifiers: chr6:g.112390639C>G (hg19) ; chr6:g.112069436C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069436C>G , CM000668.2:g.112069436C>G	GRCh38
NC_000006.11:g.112390639C>G , CM000668.1:g.112390639C>G	GRCh37
NC_000006.10:g.112497332C>G	NCBI36
NG_011748.1:g.20362C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.881C>G MANE Select	ENSP00000357655.4:p.Thr294Ser
ENST00000639360.1:c.782C>G	ENSP00000491774.1:p.Thr261Ser
ENST00000230529.9:c.881C>G	ENSP00000230529.5:p.Thr294Ser
ENST00000361714.5:c.881C>G	ENSP00000354734.2:p.Thr294Ser
ENST00000368663.4:c.*187C>G	ENSP00000357652.4:n.*187C>G
ENST00000368664.7:c.*285C>G	ENSP00000357653.3:n.*285C>G
ENST00000368666.6:c.935C>G	ENSP00000357655.3:p.Thr312Ser
ENST00000409166.5:c.209C>G	ENSP00000386467.1:p.Thr70Ser
ENST00000454589.5:c.*285C>G	ENSP00000395928.1:n.*285C>G
ENST00000604763.5:c.881C>G	ENSP00000473777.1:p.Thr294Ser
ENST00000613648.1:n.716C>G
ENST00000620524.3:n.812C>G
NM_003880.3:c.881C>G	NP_003871.1:p.Thr294Ser
NM_198239.1:c.935C>G	NP_937882.1:p.Thr312Ser
NR_125353.1:n.1135C>G
NR_125354.1:n.1055C>G
XM_011536220.1:c.881C>G	XP_011534522.1:p.Thr294Ser
XM_011536221.1:c.*285C>G	XP_011534523.1:n.*285C>G
XM_011536223.1:c.299C>G	XP_011534525.1:p.Thr100Ser
XM_011536223.3:c.299C>G	XP_011534525.1:p.Thr100Ser
XR_001743705.1:n.1483C>G
NM_003880.4:c.881C>G	NP_003871.1:p.Thr294Ser
NM_198239.2:c.881C>G MANE Select	NP_937882.2:p.Thr294Ser
NR_125353.2:n.1199C>G
NR_125354.3:n.1026C>G