Canonical Allele Identifier: CA365376885

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390780G>T (hg19) ; chr6:g.112069577G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069577G>T , CM000668.2:g.112069577G>T	GRCh38
NC_000006.11:g.112390780G>T , CM000668.1:g.112390780G>T	GRCh37
NC_000006.10:g.112497473G>T	NCBI36
NG_011748.1:g.20503G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1022G>T MANE Select	ENSP00000357655.4:p.Cys341Phe
ENST00000639360.1:c.923G>T	ENSP00000491774.1:p.Cys308Phe
ENST00000230529.9:c.1022G>T	ENSP00000230529.5:p.Cys341Phe
ENST00000361714.5:c.1022G>T	ENSP00000354734.2:p.Cys341Phe
ENST00000368663.4:c.*328G>T	ENSP00000357652.4:n.*328G>T
ENST00000368664.7:c.*426G>T	ENSP00000357653.3:n.*426G>T
ENST00000368666.6:c.1076G>T	ENSP00000357655.3:p.Cys359Phe
ENST00000409166.5:c.350G>T	ENSP00000386467.1:p.Cys117Phe
ENST00000454589.5:c.*426G>T	ENSP00000395928.1:n.*426G>T
ENST00000604763.5:c.1022G>T	ENSP00000473777.1:p.Cys341Phe
ENST00000613648.1:n.857G>T
ENST00000620524.3:n.953G>T
NM_003880.3:c.1022G>T	NP_003871.1:p.Cys341Phe
NM_198239.1:c.1076G>T	NP_937882.1:p.Cys359Phe
NR_125353.1:n.1276G>T
NR_125354.1:n.1196G>T
XM_011536220.1:c.1022G>T	XP_011534522.1:p.Cys341Phe
XM_011536221.1:c.*426G>T	XP_011534523.1:n.*426G>T
XM_011536223.1:c.440G>T	XP_011534525.1:p.Cys147Phe
XM_011536223.3:c.440G>T	XP_011534525.1:p.Cys147Phe
XR_001743705.1:n.1624G>T
NM_003880.4:c.1022G>T	NP_003871.1:p.Cys341Phe
NM_198239.2:c.1022G>T MANE Select	NP_937882.2:p.Cys341Phe
NR_125353.2:n.1340G>T
NR_125354.3:n.1167G>T