Canonical Allele Identifier: CA3964154

Gene: CCN6

Linked Data

• dbSNP Id: rs782428550
• ExAC: 6:112390848 AGTCAATCCT / A
• gnomAD v2: 6-112390848-AGTCAATCCT-A
• gnomAD v3: 6-112069645-AGTCAATCCT-A
• gnomAD v4: 6-112069645-AGTCAATCCT-A
• MyVariant Identifiers: chr6:g.112390849_112390857del (hg19) ; chr6:g.112069646_112069654del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069650_112069658del , CM000668.2:g.112069650_112069658del	GRCh38
NC_000006.11:g.112390853_112390861del , CM000668.1:g.112390853_112390861del	GRCh37
NC_000006.10:g.112497546_112497554del	NCBI36
NG_011748.1:g.20576_20584del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*30_*38del MANE Select	ENSP00000357655.4:n.*30_*38del
ENST00000639360.1:c.996_1004del	ENSP00000491774.1:n.996_1004del
ENST00000230529.9:c.*30_*38del	ENSP00000230529.5:n.*30_*38del
ENST00000361714.5:c.*30_*38del	ENSP00000354734.2:n.*30_*38del
ENST00000368664.7:c.*499_*507del	ENSP00000357653.3:n.*499_*507del
ENST00000368666.6:c.*30_*38del	ENSP00000357655.3:n.*30_*38del
ENST00000409166.5:c.*30_*38del	ENSP00000386467.1:n.*30_*38del
ENST00000454589.5:c.*499_*507del	ENSP00000395928.1:n.*499_*507del
ENST00000604763.5:c.*30_*38del	ENSP00000473777.1:n.*30_*38del
ENST00000613648.1:n.930_938del
ENST00000620524.3:n.1026_1034del
NM_003880.3:c.*30_*38del	NP_003871.1:n.*30_*38del
NM_198239.1:c.*30_*38del	NP_937882.1:n.*30_*38del
NR_125353.1:n.1349_1357del
NR_125354.1:n.1269_1277del
XM_011536220.1:c.*30_*38del	XP_011534522.1:n.*30_*38del
XM_011536221.1:c.*499_*507del	XP_011534523.1:n.*499_*507del
XM_011536223.1:c.*30_*38del	XP_011534525.1:n.*30_*38del
XM_011536223.3:c.*30_*38del	XP_011534525.1:n.*30_*38del
XR_001743705.1:n.1697_1705del
NM_003880.4:c.*30_*38del	NP_003871.1:n.*30_*38del
NM_198239.2:c.*30_*38del MANE Select	NP_937882.2:n.*30_*38del
NR_125353.2:n.1413_1421del
NR_125354.3:n.1240_1248del