Canonical Allele Identifier: CA365376982

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390794G>T (hg19) ; chr6:g.112069591G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069591G>T , CM000668.2:g.112069591G>T	GRCh38
NC_000006.11:g.112390794G>T , CM000668.1:g.112390794G>T	GRCh37
NC_000006.10:g.112497487G>T	NCBI36
NG_011748.1:g.20517G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1036G>T MANE Select	ENSP00000357655.4:p.Asp346Tyr
ENST00000639360.1:c.937G>T	ENSP00000491774.1:p.Asp313Tyr
ENST00000230529.9:c.1036G>T	ENSP00000230529.5:p.Asp346Tyr
ENST00000361714.5:c.1036G>T	ENSP00000354734.2:p.Asp346Tyr
ENST00000368663.4:c.*342G>T	ENSP00000357652.4:n.*342G>T
ENST00000368664.7:c.*440G>T	ENSP00000357653.3:n.*440G>T
ENST00000368666.6:c.1090G>T	ENSP00000357655.3:p.Asp364Tyr
ENST00000409166.5:c.364G>T	ENSP00000386467.1:p.Asp122Tyr
ENST00000454589.5:c.*440G>T	ENSP00000395928.1:n.*440G>T
ENST00000604763.5:c.1036G>T	ENSP00000473777.1:p.Asp346Tyr
ENST00000613648.1:n.871G>T
ENST00000620524.3:n.967G>T
NM_003880.3:c.1036G>T	NP_003871.1:p.Asp346Tyr
NM_198239.1:c.1090G>T	NP_937882.1:p.Asp364Tyr
NR_125353.1:n.1290G>T
NR_125354.1:n.1210G>T
XM_011536220.1:c.1036G>T	XP_011534522.1:p.Asp346Tyr
XM_011536221.1:c.*440G>T	XP_011534523.1:n.*440G>T
XM_011536223.1:c.454G>T	XP_011534525.1:p.Asp152Tyr
XM_011536223.3:c.454G>T	XP_011534525.1:p.Asp152Tyr
XR_001743705.1:n.1638G>T
NM_003880.4:c.1036G>T	NP_003871.1:p.Asp346Tyr
NM_198239.2:c.1036G>T MANE Select	NP_937882.2:p.Asp346Tyr
NR_125353.2:n.1354G>T
NR_125354.3:n.1181G>T