Canonical Allele Identifier: CA365370223

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061276G>C , CM000668.2:g.112061276G>C	GRCh38
NC_000006.11:g.112382479G>C , CM000668.1:g.112382479G>C	GRCh37
NC_000006.10:g.112489172G>C	NCBI36
NG_011748.1:g.12202G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_198239.2:c.334G>C MANE Select	NP_937882.2:p.Gly112Arg
ENST00000368666.7:c.334G>C MANE Select	ENSP00000357655.4:p.Gly112Arg
NM_003880.3:c.334G>C	NP_003871.1:p.Gly112Arg
NM_003880.4:c.334G>C	NP_003871.1:p.Gly112Arg
NM_198239.1:c.388G>C	NP_937882.1:p.Gly130Arg
NR_125353.1:n.524G>C
NR_125353.2:n.588G>C
NR_125354.1:n.444G>C
NR_125354.3:n.415G>C
ENST00000230529.9:c.334G>C	ENSP00000230529.5:p.Gly112Arg
ENST00000361714.5:c.334G>C	ENSP00000354734.2:p.Gly112Arg
ENST00000368663.4:c.334G>C	ENSP00000357652.4:p.Gly112Arg
ENST00000368664.7:c.388G>C	ENSP00000357653.3:p.Gly130Arg
ENST00000368666.6:c.388G>C	ENSP00000357655.3:p.Gly130Arg
ENST00000409166.5:c.-507-3G>C	ENSP00000386467.1:n.-507-3G>C
ENST00000454589.5:c.334G>C	ENSP00000395928.1:p.Gly112Arg
ENST00000604763.5:c.334G>C	ENSP00000473777.1:p.Gly112Arg
ENST00000620524.3:n.268G>C
ENST00000639360.1:c.238G>C	ENSP00000491774.1:p.Gly80Arg
XM_011536220.1:c.334G>C	XP_011534522.1:p.Gly112Arg
XM_011536221.1:c.397G>C	XP_011534523.1:p.Gly133Arg
XM_011536222.1:c.472G>C	XP_011534524.1:p.Gly158Arg
XM_011536222.2:c.397G>C	XP_011534524.2:p.Gly133Arg
XR_001743705.1:n.872G>C