Canonical Allele Identifier: CA2578717960

Gene: CCN6

Linked Data

• gnomAD v4: 6-112060980-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112060980A>T , CM000668.2:g.112060980A>T	GRCh38
NC_000006.11:g.112382183A>T , CM000668.1:g.112382183A>T	GRCh37
NC_000006.10:g.112488876A>T	NCBI36
NG_011748.1:g.11906A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.49-11A>T MANE Select	ENSP00000357655.4:n.49-11A>T
ENST00000230529.9:c.49-11A>T	ENSP00000230529.5:n.49-11A>T
ENST00000361714.5:c.49-11A>T	ENSP00000354734.2:n.49-11A>T
ENST00000368663.4:c.49-11A>T	ENSP00000357652.4:n.49-11A>T
ENST00000368664.7:c.103-11A>T	ENSP00000357653.3:n.103-11A>T
ENST00000368666.6:c.103-11A>T	ENSP00000357655.3:n.103-11A>T
ENST00000409166.5:c.-507-299A>T	ENSP00000386467.1:n.-507-299A>T
ENST00000454589.5:c.49-11A>T	ENSP00000395928.1:n.49-11A>T
ENST00000604763.5:c.49-11A>T	ENSP00000473777.1:n.49-11A>T
ENST00000620524.3:n.64-92A>T
NM_003880.3:c.49-11A>T	NP_003871.1:n.49-11A>T
NM_198239.1:c.103-11A>T	NP_937882.1:n.103-11A>T
NR_125353.1:n.239-11A>T
NR_125354.1:n.159-11A>T
XM_011536220.1:c.49-11A>T	XP_011534522.1:n.49-11A>T
XM_011536221.1:c.112-11A>T	XP_011534523.1:n.112-11A>T
XM_011536222.1:c.187-11A>T	XP_011534524.1:n.187-11A>T
XM_011536222.2:c.112-11A>T	XP_011534524.2:n.112-11A>T
XR_001743705.1:n.587-11A>T
NM_003880.4:c.49-11A>T	NP_003871.1:n.49-11A>T
NM_198239.2:c.49-11A>T MANE Select	NP_937882.2:n.49-11A>T
NR_125353.2:n.303-11A>T
NR_125354.3:n.130-11A>T