Canonical Allele Identifier: CA1655201642

Gene: CCN6

Linked Data

• dbSNP Id: rs1776819013
• gnomAD v4: 6-112069673-TAGTG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069677_112069680del , CM000668.2:g.112069677_112069680del	GRCh38
NC_000006.11:g.112390880_112390883del , CM000668.1:g.112390880_112390883del	GRCh37
NC_000006.10:g.112497573_112497576del	NCBI36
NG_011748.1:g.20603_20606del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*57_*60del MANE Select	ENSP00000357655.4:n.*57_*60del
ENST00000639360.1:c.1023_1026del	ENSP00000491774.1:n.1023_1026del
ENST00000230529.9:c.*57_*60del	ENSP00000230529.5:n.*57_*60del
ENST00000361714.5:c.*57_*60del	ENSP00000354734.2:n.*57_*60del
ENST00000368666.6:c.*57_*60del	ENSP00000357655.3:n.*57_*60del
ENST00000454589.5:c.*526_*529del	ENSP00000395928.1:n.*526_*529del
ENST00000604763.5:c.*57_*60del	ENSP00000473777.1:n.*57_*60del
ENST00000620524.3:n.1053_1056del
NM_003880.3:c.*57_*60del	NP_003871.1:n.*57_*60del
NM_198239.1:c.*57_*60del	NP_937882.1:n.*57_*60del
NR_125353.1:n.1376_1379del
NR_125354.1:n.1296_1299del
XM_011536220.1:c.*57_*60del	XP_011534522.1:n.*57_*60del
XM_011536221.1:c.*526_*529del	XP_011534523.1:n.*526_*529del
XM_011536223.1:c.*57_*60del	XP_011534525.1:n.*57_*60del
XM_011536223.3:c.*57_*60del	XP_011534525.1:n.*57_*60del
XR_001743705.1:n.1724_1727del
NM_003880.4:c.*57_*60del	NP_003871.1:n.*57_*60del
NM_198239.2:c.*57_*60del MANE Select	NP_937882.2:n.*57_*60del
NR_125353.2:n.1440_1443del
NR_125354.3:n.1267_1270del