Canonical Allele Identifier: CA365376395

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390706A>T (hg19) ; chr6:g.112069503A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069503A>T , CM000668.2:g.112069503A>T	GRCh38
NC_000006.11:g.112390706A>T , CM000668.1:g.112390706A>T	GRCh37
NC_000006.10:g.112497399A>T	NCBI36
NG_011748.1:g.20429A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.948A>T MANE Select	ENSP00000357655.4:p.Gln316His
ENST00000639360.1:c.849A>T	ENSP00000491774.1:p.Gln283His
ENST00000230529.9:c.948A>T	ENSP00000230529.5:p.Gln316His
ENST00000361714.5:c.948A>T	ENSP00000354734.2:p.Gln316His
ENST00000368663.4:c.*254A>T	ENSP00000357652.4:n.*254A>T
ENST00000368664.7:c.*352A>T	ENSP00000357653.3:n.*352A>T
ENST00000368666.6:c.1002A>T	ENSP00000357655.3:p.Gln334His
ENST00000409166.5:c.276A>T	ENSP00000386467.1:p.Gln92His
ENST00000454589.5:c.*352A>T	ENSP00000395928.1:n.*352A>T
ENST00000604763.5:c.948A>T	ENSP00000473777.1:p.Gln316His
ENST00000613648.1:n.783A>T
ENST00000620524.3:n.879A>T
NM_003880.3:c.948A>T	NP_003871.1:p.Gln316His
NM_198239.1:c.1002A>T	NP_937882.1:p.Gln334His
NR_125353.1:n.1202A>T
NR_125354.1:n.1122A>T
XM_011536220.1:c.948A>T	XP_011534522.1:p.Gln316His
XM_011536221.1:c.*352A>T	XP_011534523.1:n.*352A>T
XM_011536223.1:c.366A>T	XP_011534525.1:p.Gln122His
XM_011536223.3:c.366A>T	XP_011534525.1:p.Gln122His
XR_001743705.1:n.1550A>T
NM_003880.4:c.948A>T	NP_003871.1:p.Gln316His
NM_198239.2:c.948A>T MANE Select	NP_937882.2:p.Gln316His
NR_125353.2:n.1266A>T
NR_125354.3:n.1093A>T