Canonical Allele Identifier: CA1655198669

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061174T= , CM000668.2:g.112061174T=	GRCh38
NC_000006.11:g.112382377T= , CM000668.1:g.112382377T=	GRCh37
NC_000006.10:g.112489070T=	NCBI36
NG_011748.1:g.12100T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.232T= MANE Select	ENSP00000357655.4:p.Cys78=
ENST00000639360.1:c.136T=	ENSP00000491774.1:p.Cys46=
ENST00000230529.9:c.232T=	ENSP00000230529.5:p.Cys78=
ENST00000361714.5:c.232T=	ENSP00000354734.2:p.Cys78=
ENST00000368663.4:c.232T=	ENSP00000357652.4:p.Cys78=
ENST00000368664.7:c.286T=	ENSP00000357653.3:p.Cys96=
ENST00000368666.6:c.286T=	ENSP00000357655.3:p.Cys96=
ENST00000409166.5:c.-507-105T=	ENSP00000386467.1:n.-507-105T=
ENST00000454589.5:c.232T=	ENSP00000395928.1:p.Cys78=
ENST00000604763.5:c.232T=	ENSP00000473777.1:p.Cys78=
ENST00000620524.3:n.166T=
NM_003880.3:c.232T=	NP_003871.1:p.Cys78=
NM_198239.1:c.286T=	NP_937882.1:p.Cys96=
NR_125353.1:n.422T=
NR_125354.1:n.342T=
XM_011536220.1:c.232T=	XP_011534522.1:p.Cys78=
XM_011536221.1:c.295T=	XP_011534523.1:p.Cys99=
XM_011536222.1:c.370T=	XP_011534524.1:p.Cys124=
XM_011536222.2:c.295T=	XP_011534524.2:p.Cys99=
XR_001743705.1:n.770T=
NM_003880.4:c.232T=	NP_003871.1:p.Cys78=
NM_198239.2:c.232T= MANE Select	NP_937882.2:p.Cys78=
NR_125353.2:n.486T=
NR_125354.3:n.313T=