Canonical Allele Identifier: CA2680044661

Gene: CCN6

Linked Data

• gnomAD v4: 6-112061074-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061077dup , CM000668.2:g.112061077dup	GRCh38
NC_000006.11:g.112382280dup , CM000668.1:g.112382280dup	GRCh37
NC_000006.10:g.112488973dup	NCBI36
NG_011748.1:g.12003dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.135dup MANE Select	ENSP00000357655.4:p.Gln46ThrfsTer?
ENST00000639360.1:c.39dup	ENSP00000491774.1:p.Gln14ThrfsTer?
ENST00000230529.9:c.135dup	ENSP00000230529.5:p.Gln46ThrfsTer?
ENST00000361714.5:c.135dup	ENSP00000354734.2:p.Gln46ThrfsTer?
ENST00000368663.4:c.135dup	ENSP00000357652.4:p.Gln46ThrfsTer?
ENST00000368664.7:c.189dup	ENSP00000357653.3:p.Gln64ThrfsTer?
ENST00000368666.6:c.189dup	ENSP00000357655.3:p.Gln64ThrfsTer?
ENST00000409166.5:c.-507-202dup	ENSP00000386467.1:n.-507-202dup
ENST00000454589.5:c.135dup	ENSP00000395928.1:p.Gln46ThrfsTer?
ENST00000604763.5:c.135dup	ENSP00000473777.1:p.Gln46ThrfsTer?
ENST00000620524.3:n.69dup
NM_003880.3:c.135dup	NP_003871.1:p.Gln46ThrfsTer?
NM_198239.1:c.189dup	NP_937882.1:p.Gln64ThrfsTer?
NR_125353.1:n.325dup
NR_125354.1:n.245dup
XM_011536220.1:c.135dup	XP_011534522.1:p.Gln46ThrfsTer?
XM_011536221.1:c.198dup	XP_011534523.1:p.Gln67ThrfsTer?
XM_011536222.1:c.273dup	XP_011534524.1:p.Gln92ThrfsTer?
XM_011536222.2:c.198dup	XP_011534524.2:p.Gln67ThrfsTer?
XR_001743705.1:n.673dup
NM_003880.4:c.135dup	NP_003871.1:p.Gln46ThrfsTer?
NM_198239.2:c.135dup MANE Select	NP_937882.2:p.Gln46ThrfsTer?
NR_125353.2:n.389dup
NR_125354.3:n.216dup