Canonical Allele Identifier: CA2680045428

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069664-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069671dup , CM000668.2:g.112069671dup	GRCh38
NC_000006.11:g.112390874dup , CM000668.1:g.112390874dup	GRCh37
NC_000006.10:g.112497567dup	NCBI36
NG_011748.1:g.20597dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*51dup MANE Select	ENSP00000357655.4:n.*51dup
ENST00000639360.1:c.1017dup	ENSP00000491774.1:n.1017dup
ENST00000230529.9:c.*51dup	ENSP00000230529.5:n.*51dup
ENST00000361714.5:c.*51dup	ENSP00000354734.2:n.*51dup
ENST00000368666.6:c.*51dup	ENSP00000357655.3:n.*51dup
ENST00000454589.5:c.*520dup	ENSP00000395928.1:n.*520dup
ENST00000604763.5:c.*51dup	ENSP00000473777.1:n.*51dup
ENST00000620524.3:n.1047dup
NM_003880.3:c.*51dup	NP_003871.1:n.*51dup
NM_198239.1:c.*51dup	NP_937882.1:n.*51dup
NR_125353.1:n.1370dup
NR_125354.1:n.1290dup
XM_011536220.1:c.*51dup	XP_011534522.1:n.*51dup
XM_011536221.1:c.*520dup	XP_011534523.1:n.*520dup
XM_011536223.1:c.*51dup	XP_011534525.1:n.*51dup
XM_011536223.3:c.*51dup	XP_011534525.1:n.*51dup
XR_001743705.1:n.1718dup
NM_003880.4:c.*51dup	NP_003871.1:n.*51dup
NM_198239.2:c.*51dup MANE Select	NP_937882.2:n.*51dup
NR_125353.2:n.1434dup
NR_125354.3:n.1261dup