Canonical Allele Identifier: CA1655201648

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069682T= , CM000668.2:g.112069682T=	GRCh38
NC_000006.11:g.112390885T= , CM000668.1:g.112390885T=	GRCh37
NC_000006.10:g.112497578T=	NCBI36
NG_011748.1:g.20608T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*62T= MANE Select	ENSP00000357655.4:n.*62T=
ENST00000361714.5:c.*62T=	ENSP00000354734.2:n.*62T=
ENST00000368666.6:c.*62T=	ENSP00000357655.3:n.*62T=
ENST00000454589.5:c.*531T=	ENSP00000395928.1:n.*531T=
ENST00000604763.5:c.*62T=	ENSP00000473777.1:n.*62T=
ENST00000620524.3:n.1058T=
NM_003880.3:c.*62T=	NP_003871.1:n.*62T=
NM_198239.1:c.*62T=	NP_937882.1:n.*62T=
NR_125353.1:n.1381T=
NR_125354.1:n.1301T=
XM_011536220.1:c.*62T=	XP_011534522.1:n.*62T=
XM_011536221.1:c.*531T=	XP_011534523.1:n.*531T=
XM_011536223.1:c.*62T=	XP_011534525.1:n.*62T=
XM_011536223.3:c.*62T=	XP_011534525.1:n.*62T=
XR_001743705.1:n.1729T=
NM_003880.4:c.*62T=	NP_003871.1:n.*62T=
NM_198239.2:c.*62T= MANE Select	NP_937882.2:n.*62T=
NR_125353.2:n.1445T=
NR_125354.3:n.1272T=