Canonical Allele Identifier: CA1655201643

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069674A= , CM000668.2:g.112069674A=	GRCh38
NC_000006.11:g.112390877A= , CM000668.1:g.112390877A=	GRCh37
NC_000006.10:g.112497570A=	NCBI36
NG_011748.1:g.20600A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*54A= MANE Select	ENSP00000357655.4:n.*54A=
ENST00000639360.1:c.1020A=	ENSP00000491774.1:n.1020A=
ENST00000230529.9:c.*54A=	ENSP00000230529.5:n.*54A=
ENST00000361714.5:c.*54A=	ENSP00000354734.2:n.*54A=
ENST00000368666.6:c.*54A=	ENSP00000357655.3:n.*54A=
ENST00000454589.5:c.*523A=	ENSP00000395928.1:n.*523A=
ENST00000604763.5:c.*54A=	ENSP00000473777.1:n.*54A=
ENST00000620524.3:n.1050A=
NM_003880.3:c.*54A=	NP_003871.1:n.*54A=
NM_198239.1:c.*54A=	NP_937882.1:n.*54A=
NR_125353.1:n.1373A=
NR_125354.1:n.1293A=
XM_011536220.1:c.*54A=	XP_011534522.1:n.*54A=
XM_011536221.1:c.*523A=	XP_011534523.1:n.*523A=
XM_011536223.1:c.*54A=	XP_011534525.1:n.*54A=
XM_011536223.3:c.*54A=	XP_011534525.1:n.*54A=
XR_001743705.1:n.1721A=
NM_003880.4:c.*54A=	NP_003871.1:n.*54A=
NM_198239.2:c.*54A= MANE Select	NP_937882.2:n.*54A=
NR_125353.2:n.1437A=
NR_125354.3:n.1264A=