Canonical Allele Identifier: CA365376969

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390791G>A (hg19) ; chr6:g.112069588G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069588G>A , CM000668.2:g.112069588G>A	GRCh38
NC_000006.11:g.112390791G>A , CM000668.1:g.112390791G>A	GRCh37
NC_000006.10:g.112497484G>A	NCBI36
NG_011748.1:g.20514G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1033G>A MANE Select	ENSP00000357655.4:p.Gly345Arg
ENST00000639360.1:c.934G>A	ENSP00000491774.1:p.Gly312Arg
ENST00000230529.9:c.1033G>A	ENSP00000230529.5:p.Gly345Arg
ENST00000361714.5:c.1033G>A	ENSP00000354734.2:p.Gly345Arg
ENST00000368663.4:c.*339G>A	ENSP00000357652.4:n.*339G>A
ENST00000368664.7:c.*437G>A	ENSP00000357653.3:n.*437G>A
ENST00000368666.6:c.1087G>A	ENSP00000357655.3:p.Gly363Arg
ENST00000409166.5:c.361G>A	ENSP00000386467.1:p.Gly121Arg
ENST00000454589.5:c.*437G>A	ENSP00000395928.1:n.*437G>A
ENST00000604763.5:c.1033G>A	ENSP00000473777.1:p.Gly345Arg
ENST00000613648.1:n.868G>A
ENST00000620524.3:n.964G>A
NM_003880.3:c.1033G>A	NP_003871.1:p.Gly345Arg
NM_198239.1:c.1087G>A	NP_937882.1:p.Gly363Arg
NR_125353.1:n.1287G>A
NR_125354.1:n.1207G>A
XM_011536220.1:c.1033G>A	XP_011534522.1:p.Gly345Arg
XM_011536221.1:c.*437G>A	XP_011534523.1:n.*437G>A
XM_011536223.1:c.451G>A	XP_011534525.1:p.Gly151Arg
XM_011536223.3:c.451G>A	XP_011534525.1:p.Gly151Arg
XR_001743705.1:n.1635G>A
NM_003880.4:c.1033G>A	NP_003871.1:p.Gly345Arg
NM_198239.2:c.1033G>A MANE Select	NP_937882.2:p.Gly345Arg
NR_125353.2:n.1351G>A
NR_125354.3:n.1178G>A