Canonical Allele Identifier: CA2680045434

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069679-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069679G>C , CM000668.2:g.112069679G>C	GRCh38
NC_000006.11:g.112390882G>C , CM000668.1:g.112390882G>C	GRCh37
NC_000006.10:g.112497575G>C	NCBI36
NG_011748.1:g.20605G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*59G>C MANE Select	ENSP00000357655.4:n.*59G>C
ENST00000639360.1:c.1025G>C	ENSP00000491774.1:n.1025G>C
ENST00000230529.9:c.*59G>C	ENSP00000230529.5:n.*59G>C
ENST00000361714.5:c.*59G>C	ENSP00000354734.2:n.*59G>C
ENST00000368666.6:c.*59G>C	ENSP00000357655.3:n.*59G>C
ENST00000454589.5:c.*528G>C	ENSP00000395928.1:n.*528G>C
ENST00000604763.5:c.*59G>C	ENSP00000473777.1:n.*59G>C
ENST00000620524.3:n.1055G>C
NM_003880.3:c.*59G>C	NP_003871.1:n.*59G>C
NM_198239.1:c.*59G>C	NP_937882.1:n.*59G>C
NR_125353.1:n.1378G>C
NR_125354.1:n.1298G>C
XM_011536220.1:c.*59G>C	XP_011534522.1:n.*59G>C
XM_011536221.1:c.*528G>C	XP_011534523.1:n.*528G>C
XM_011536223.1:c.*59G>C	XP_011534525.1:n.*59G>C
XM_011536223.3:c.*59G>C	XP_011534525.1:n.*59G>C
XR_001743705.1:n.1726G>C
NM_003880.4:c.*59G>C	NP_003871.1:n.*59G>C
NM_198239.2:c.*59G>C MANE Select	NP_937882.2:n.*59G>C
NR_125353.2:n.1442G>C
NR_125354.3:n.1269G>C