Canonical Allele Identifier: CA2680045408

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069490-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069491del , CM000668.2:g.112069491del	GRCh38
NC_000006.11:g.112390694del , CM000668.1:g.112390694del	GRCh37
NC_000006.10:g.112497387del	NCBI36
NG_011748.1:g.20417del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.936del MANE Select	ENSP00000357655.4:p.Met312IlefsTer?
ENST00000639360.1:c.837del	ENSP00000491774.1:p.Met279IlefsTer?
ENST00000230529.9:c.936del	ENSP00000230529.5:p.Met312IlefsTer?
ENST00000361714.5:c.936del	ENSP00000354734.2:p.Met312IlefsTer?
ENST00000368663.4:c.*242del	ENSP00000357652.4:n.*242del
ENST00000368664.7:c.*340del	ENSP00000357653.3:n.*340del
ENST00000368666.6:c.990del	ENSP00000357655.3:p.Met330IlefsTer?
ENST00000409166.5:c.264del	ENSP00000386467.1:p.Met88IlefsTer?
ENST00000454589.5:c.*340del	ENSP00000395928.1:n.*340del
ENST00000604763.5:c.936del	ENSP00000473777.1:p.Met312IlefsTer?
ENST00000613648.1:n.771del
ENST00000620524.3:n.867del
NM_003880.3:c.936del	NP_003871.1:p.Met312IlefsTer?
NM_198239.1:c.990del	NP_937882.1:p.Met330IlefsTer?
NR_125353.1:n.1190del
NR_125354.1:n.1110del
XM_011536220.1:c.936del	XP_011534522.1:p.Met312IlefsTer?
XM_011536221.1:c.*340del	XP_011534523.1:n.*340del
XM_011536223.1:c.354del	XP_011534525.1:p.Met118IlefsTer?
XM_011536223.3:c.354del	XP_011534525.1:p.Met118IlefsTer?
XR_001743705.1:n.1538del
NM_003880.4:c.936del	NP_003871.1:p.Met312IlefsTer?
NM_198239.2:c.936del MANE Select	NP_937882.2:p.Met312IlefsTer?
NR_125353.2:n.1254del
NR_125354.3:n.1081del