Canonical Allele Identifier: CA1655201594

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069557T= , CM000668.2:g.112069557T=	GRCh38
NC_000006.11:g.112390760T= , CM000668.1:g.112390760T=	GRCh37
NC_000006.10:g.112497453T=	NCBI36
NG_011748.1:g.20483T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1002T= MANE Select	ENSP00000357655.4:p.Ser334=
ENST00000639360.1:c.903T=	ENSP00000491774.1:p.Ser301=
ENST00000230529.9:c.1002T=	ENSP00000230529.5:p.Ser334=
ENST00000361714.5:c.1002T=	ENSP00000354734.2:p.Ser334=
ENST00000368663.4:c.*308T=	ENSP00000357652.4:n.*308T=
ENST00000368664.7:c.*406T=	ENSP00000357653.3:n.*406T=
ENST00000368666.6:c.1056T=	ENSP00000357655.3:p.Ser352=
ENST00000409166.5:c.330T=	ENSP00000386467.1:p.Ser110=
ENST00000454589.5:c.*406T=	ENSP00000395928.1:n.*406T=
ENST00000604763.5:c.1002T=	ENSP00000473777.1:p.Ser334=
ENST00000613648.1:n.837T=
ENST00000620524.3:n.933T=
NM_003880.3:c.1002T=	NP_003871.1:p.Ser334=
NM_198239.1:c.1056T=	NP_937882.1:p.Ser352=
NR_125353.1:n.1256T=
NR_125354.1:n.1176T=
XM_011536220.1:c.1002T=	XP_011534522.1:p.Ser334=
XM_011536221.1:c.*406T=	XP_011534523.1:n.*406T=
XM_011536223.1:c.420T=	XP_011534525.1:p.Ser140=
XM_011536223.3:c.420T=	XP_011534525.1:p.Ser140=
XR_001743705.1:n.1604T=
NM_003880.4:c.1002T=	NP_003871.1:p.Ser334=
NM_198239.2:c.1002T= MANE Select	NP_937882.2:p.Ser334=
NR_125353.2:n.1320T=
NR_125354.3:n.1147T=