Canonical Allele Identifier: CA2680045427

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069664-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069664T>C , CM000668.2:g.112069664T>C	GRCh38
NC_000006.11:g.112390867T>C , CM000668.1:g.112390867T>C	GRCh37
NC_000006.10:g.112497560T>C	NCBI36
NG_011748.1:g.20590T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*44T>C MANE Select	ENSP00000357655.4:n.*44T>C
ENST00000639360.1:c.1010T>C	ENSP00000491774.1:n.1010T>C
ENST00000230529.9:c.*44T>C	ENSP00000230529.5:n.*44T>C
ENST00000361714.5:c.*44T>C	ENSP00000354734.2:n.*44T>C
ENST00000368666.6:c.*44T>C	ENSP00000357655.3:n.*44T>C
ENST00000454589.5:c.*513T>C	ENSP00000395928.1:n.*513T>C
ENST00000604763.5:c.*44T>C	ENSP00000473777.1:n.*44T>C
ENST00000620524.3:n.1040T>C
NM_003880.3:c.*44T>C	NP_003871.1:n.*44T>C
NM_198239.1:c.*44T>C	NP_937882.1:n.*44T>C
NR_125353.1:n.1363T>C
NR_125354.1:n.1283T>C
XM_011536220.1:c.*44T>C	XP_011534522.1:n.*44T>C
XM_011536221.1:c.*513T>C	XP_011534523.1:n.*513T>C
XM_011536223.1:c.*44T>C	XP_011534525.1:n.*44T>C
XM_011536223.3:c.*44T>C	XP_011534525.1:n.*44T>C
XR_001743705.1:n.1711T>C
NM_003880.4:c.*44T>C	NP_003871.1:n.*44T>C
NM_198239.2:c.*44T>C MANE Select	NP_937882.2:n.*44T>C
NR_125353.2:n.1427T>C
NR_125354.3:n.1254T>C