Canonical Allele Identifier: CA1655198671

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061179C= , CM000668.2:g.112061179C=	GRCh38
NC_000006.11:g.112382382C= , CM000668.1:g.112382382C=	GRCh37
NC_000006.10:g.112489075C=	NCBI36
NG_011748.1:g.12105C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.237C= MANE Select	ENSP00000357655.4:p.Ala79=
ENST00000639360.1:c.141C=	ENSP00000491774.1:p.Ala47=
ENST00000230529.9:c.237C=	ENSP00000230529.5:p.Ala79=
ENST00000361714.5:c.237C=	ENSP00000354734.2:p.Ala79=
ENST00000368663.4:c.237C=	ENSP00000357652.4:p.Ala79=
ENST00000368664.7:c.291C=	ENSP00000357653.3:p.Ala97=
ENST00000368666.6:c.291C=	ENSP00000357655.3:p.Ala97=
ENST00000409166.5:c.-507-100C=	ENSP00000386467.1:n.-507-100C=
ENST00000454589.5:c.237C=	ENSP00000395928.1:p.Ala79=
ENST00000604763.5:c.237C=	ENSP00000473777.1:p.Ala79=
ENST00000620524.3:n.171C=
NM_003880.3:c.237C=	NP_003871.1:p.Ala79=
NM_198239.1:c.291C=	NP_937882.1:p.Ala97=
NR_125353.1:n.427C=
NR_125354.1:n.347C=
XM_011536220.1:c.237C=	XP_011534522.1:p.Ala79=
XM_011536221.1:c.300C=	XP_011534523.1:p.Ala100=
XM_011536222.1:c.375C=	XP_011534524.1:p.Ala125=
XM_011536222.2:c.300C=	XP_011534524.2:p.Ala100=
XR_001743705.1:n.775C=
NM_003880.4:c.237C=	NP_003871.1:p.Ala79=
NM_198239.2:c.237C= MANE Select	NP_937882.2:p.Ala79=
NR_125353.2:n.491C=
NR_125354.3:n.318C=