Canonical Allele Identifier: CA1655198632

Gene: CCN6

Linked Data

• dbSNP Id: rs1776503910

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061095del , CM000668.2:g.112061095del	GRCh38
NC_000006.11:g.112382298del , CM000668.1:g.112382298del	GRCh37
NC_000006.10:g.112488991del	NCBI36
NG_011748.1:g.12021del

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.153del MANE Select	ENSP00000357655.4:p.Cys52AlafsTer14
ENST00000639360.1:c.57del	ENSP00000491774.1:p.Cys20AlafsTer14
ENST00000230529.9:c.153del	ENSP00000230529.5:p.Cys52AlafsTer14
ENST00000361714.5:c.153del	ENSP00000354734.2:p.Cys52AlafsTer14
ENST00000368663.4:c.153del	ENSP00000357652.4:p.Cys52AlafsTer14
ENST00000368664.7:c.207del	ENSP00000357653.3:p.Cys70AlafsTer14
ENST00000368666.6:c.207del	ENSP00000357655.3:p.Cys70AlafsTer14
ENST00000409166.5:c.-507-184del	ENSP00000386467.1:n.-507-184del
ENST00000454589.5:c.153del	ENSP00000395928.1:p.Cys52AlafsTer14
ENST00000604763.5:c.153del	ENSP00000473777.1:p.Cys52AlafsTer14
ENST00000620524.3:n.87del
NM_003880.3:c.153del	NP_003871.1:p.Cys52AlafsTer14
NM_198239.1:c.207del	NP_937882.1:p.Cys70AlafsTer14
NR_125353.1:n.343del
NR_125354.1:n.263del
XM_011536220.1:c.153del	XP_011534522.1:p.Cys52AlafsTer14
XM_011536221.1:c.216del	XP_011534523.1:p.Cys73AlafsTer14
XM_011536222.1:c.291del	XP_011534524.1:p.Cys98AlafsTer14
XM_011536222.2:c.216del	XP_011534524.2:p.Cys73AlafsTer14
XR_001743705.1:n.691del
NM_003880.4:c.153del	NP_003871.1:p.Cys52AlafsTer14
NM_198239.2:c.153del MANE Select	NP_937882.2:p.Cys52AlafsTer14
NR_125353.2:n.407del
NR_125354.3:n.234del