Canonical Allele Identifier: CA365376818

Gene: CCN6

Linked Data

• COSMIC: COSM167866
• MyVariant Identifiers: chr6:g.112390774G>T (hg19) ; chr6:g.112069571G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069571G>T , CM000668.2:g.112069571G>T	GRCh38
NC_000006.11:g.112390774G>T , CM000668.1:g.112390774G>T	GRCh37
NC_000006.10:g.112497467G>T	NCBI36
NG_011748.1:g.20497G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1016G>T MANE Select	ENSP00000357655.4:p.Arg339Ile
ENST00000639360.1:c.917G>T	ENSP00000491774.1:p.Arg306Ile
ENST00000230529.9:c.1016G>T	ENSP00000230529.5:p.Arg339Ile
ENST00000361714.5:c.1016G>T	ENSP00000354734.2:p.Arg339Ile
ENST00000368663.4:c.*322G>T	ENSP00000357652.4:n.*322G>T
ENST00000368664.7:c.*420G>T	ENSP00000357653.3:n.*420G>T
ENST00000368666.6:c.1070G>T	ENSP00000357655.3:p.Arg357Ile
ENST00000409166.5:c.344G>T	ENSP00000386467.1:p.Arg115Ile
ENST00000454589.5:c.*420G>T	ENSP00000395928.1:n.*420G>T
ENST00000604763.5:c.1016G>T	ENSP00000473777.1:p.Arg339Ile
ENST00000613648.1:n.851G>T
ENST00000620524.3:n.947G>T
NM_003880.3:c.1016G>T	NP_003871.1:p.Arg339Ile
NM_198239.1:c.1070G>T	NP_937882.1:p.Arg357Ile
NR_125353.1:n.1270G>T
NR_125354.1:n.1190G>T
XM_011536220.1:c.1016G>T	XP_011534522.1:p.Arg339Ile
XM_011536221.1:c.*420G>T	XP_011534523.1:n.*420G>T
XM_011536223.1:c.434G>T	XP_011534525.1:p.Arg145Ile
XM_011536223.3:c.434G>T	XP_011534525.1:p.Arg145Ile
XR_001743705.1:n.1618G>T
NM_003880.4:c.1016G>T	NP_003871.1:p.Arg339Ile
NM_198239.2:c.1016G>T MANE Select	NP_937882.2:p.Arg339Ile
NR_125353.2:n.1334G>T
NR_125354.3:n.1161G>T