Canonical Allele Identifier: CA1655201620

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069637_112069638delinsGA , CM000668.2:g.112069637_112069638delinsGA	GRCh38
NC_000006.11:g.112390840_112390841delinsGA , CM000668.1:g.112390840_112390841delinsGA	GRCh37
NC_000006.10:g.112497533_112497534delinsGA	NCBI36
NG_011748.1:g.20563_20564delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*17_*18delinsGA MANE Select	ENSP00000357655.4:n.*17_*18delinsGA
ENST00000639360.1:c.983_984delinsGA	ENSP00000491774.1:n.983_984delinsGA
ENST00000230529.9:c.*17_*18delinsGA	ENSP00000230529.5:n.*17_*18delinsGA
ENST00000361714.5:c.*17_*18delinsGA	ENSP00000354734.2:n.*17_*18delinsGA
ENST00000368663.4:c.*388_*389delinsGA	ENSP00000357652.4:n.*388_*389delinsGA
ENST00000368664.7:c.*486_*487delinsGA	ENSP00000357653.3:n.*486_*487delinsGA
ENST00000368666.6:c.*17_*18delinsGA	ENSP00000357655.3:n.*17_*18delinsGA
ENST00000409166.5:c.*17_*18delinsGA	ENSP00000386467.1:n.*17_*18delinsGA
ENST00000454589.5:c.*486_*487delinsGA	ENSP00000395928.1:n.*486_*487delinsGA
ENST00000604763.5:c.*17_*18delinsGA	ENSP00000473777.1:n.*17_*18delinsGA
ENST00000613648.1:n.917_918delinsGA
ENST00000620524.3:n.1013_1014delinsGA
NM_003880.3:c.*17_*18delinsGA	NP_003871.1:n.*17_*18delinsGA
NM_198239.1:c.*17_*18delinsGA	NP_937882.1:n.*17_*18delinsGA
NR_125353.1:n.1336_1337delinsGA
NR_125354.1:n.1256_1257delinsGA
XM_011536220.1:c.*17_*18delinsGA	XP_011534522.1:n.*17_*18delinsGA
XM_011536221.1:c.*486_*487delinsGA	XP_011534523.1:n.*486_*487delinsGA
XM_011536223.1:c.*17_*18delinsGA	XP_011534525.1:n.*17_*18delinsGA
XM_011536223.3:c.*17_*18delinsGA	XP_011534525.1:n.*17_*18delinsGA
XR_001743705.1:n.1684_1685delinsGA
NM_003880.4:c.*17_*18delinsGA	NP_003871.1:n.*17_*18delinsGA
NM_198239.2:c.*17_*18delinsGA MANE Select	NP_937882.2:n.*17_*18delinsGA
NR_125353.2:n.1400_1401delinsGA
NR_125354.3:n.1227_1228delinsGA