Canonical Allele Identifier: CA2680045432

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069676-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069676T>G , CM000668.2:g.112069676T>G	GRCh38
NC_000006.11:g.112390879T>G , CM000668.1:g.112390879T>G	GRCh37
NC_000006.10:g.112497572T>G	NCBI36
NG_011748.1:g.20602T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*56T>G MANE Select	ENSP00000357655.4:n.*56T>G
ENST00000639360.1:c.1022T>G	ENSP00000491774.1:n.1022T>G
ENST00000230529.9:c.*56T>G	ENSP00000230529.5:n.*56T>G
ENST00000361714.5:c.*56T>G	ENSP00000354734.2:n.*56T>G
ENST00000368666.6:c.*56T>G	ENSP00000357655.3:n.*56T>G
ENST00000454589.5:c.*525T>G	ENSP00000395928.1:n.*525T>G
ENST00000604763.5:c.*56T>G	ENSP00000473777.1:n.*56T>G
ENST00000620524.3:n.1052T>G
NM_003880.3:c.*56T>G	NP_003871.1:n.*56T>G
NM_198239.1:c.*56T>G	NP_937882.1:n.*56T>G
NR_125353.1:n.1375T>G
NR_125354.1:n.1295T>G
XM_011536220.1:c.*56T>G	XP_011534522.1:n.*56T>G
XM_011536221.1:c.*525T>G	XP_011534523.1:n.*525T>G
XM_011536223.1:c.*56T>G	XP_011534525.1:n.*56T>G
XM_011536223.3:c.*56T>G	XP_011534525.1:n.*56T>G
XR_001743705.1:n.1723T>G
NM_003880.4:c.*56T>G	NP_003871.1:n.*56T>G
NM_198239.2:c.*56T>G MANE Select	NP_937882.2:n.*56T>G
NR_125353.2:n.1439T>G
NR_125354.3:n.1266T>G