Canonical Allele Identifier: CA2772632799

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069634G>T , CM000668.2:g.112069634G>T	GRCh38
NC_000006.11:g.112390837G>T , CM000668.1:g.112390837G>T	GRCh37
NC_000006.10:g.112497530G>T	NCBI36
NG_011748.1:g.20560G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*14G>T MANE Select	ENSP00000357655.4:n.*14G>T
ENST00000639360.1:c.980G>T	ENSP00000491774.1:n.980G>T
ENST00000230529.9:c.*14G>T	ENSP00000230529.5:n.*14G>T
ENST00000361714.5:c.*14G>T	ENSP00000354734.2:n.*14G>T
ENST00000368663.4:c.*385G>T	ENSP00000357652.4:n.*385G>T
ENST00000368664.7:c.*483G>T	ENSP00000357653.3:n.*483G>T
ENST00000368666.6:c.*14G>T	ENSP00000357655.3:n.*14G>T
ENST00000409166.5:c.*14G>T	ENSP00000386467.1:n.*14G>T
ENST00000454589.5:c.*483G>T	ENSP00000395928.1:n.*483G>T
ENST00000604763.5:c.*14G>T	ENSP00000473777.1:n.*14G>T
ENST00000613648.1:n.914G>T
ENST00000620524.3:n.1010G>T
NM_003880.3:c.*14G>T	NP_003871.1:n.*14G>T
NM_198239.1:c.*14G>T	NP_937882.1:n.*14G>T
NR_125353.1:n.1333G>T
NR_125354.1:n.1253G>T
XM_011536220.1:c.*14G>T	XP_011534522.1:n.*14G>T
XM_011536221.1:c.*483G>T	XP_011534523.1:n.*483G>T
XM_011536223.1:c.*14G>T	XP_011534525.1:n.*14G>T
XM_011536223.3:c.*14G>T	XP_011534525.1:n.*14G>T
XR_001743705.1:n.1681G>T
NM_003880.4:c.*14G>T	NP_003871.1:n.*14G>T
NM_198239.2:c.*14G>T MANE Select	NP_937882.2:n.*14G>T
NR_125353.2:n.1397G>T
NR_125354.3:n.1224G>T