Canonical Allele Identifier: CA451901330

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390646T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069443T>C , CM000668.2:g.112069443T>C	GRCh38
NC_000006.11:g.112390646T>C , CM000668.1:g.112390646T>C	GRCh37
NC_000006.10:g.112497339T>C	NCBI36
NG_011748.1:g.20369T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.888T>C MANE Select	ENSP00000357655.4:p.Cys296=
ENST00000639360.1:c.789T>C	ENSP00000491774.1:p.Cys263=
ENST00000230529.9:c.888T>C	ENSP00000230529.5:p.Cys296=
ENST00000361714.5:c.888T>C	ENSP00000354734.2:p.Cys296=
ENST00000368663.4:c.*194T>C	ENSP00000357652.4:n.*194T>C
ENST00000368664.7:c.*292T>C	ENSP00000357653.3:n.*292T>C
ENST00000368666.6:c.942T>C	ENSP00000357655.3:p.Cys314=
ENST00000409166.5:c.216T>C	ENSP00000386467.1:p.Cys72=
ENST00000454589.5:c.*292T>C	ENSP00000395928.1:n.*292T>C
ENST00000604763.5:c.888T>C	ENSP00000473777.1:p.Cys296=
ENST00000613648.1:n.723T>C
ENST00000620524.3:n.819T>C
NM_003880.3:c.888T>C	NP_003871.1:p.Cys296=
NM_198239.1:c.942T>C	NP_937882.1:p.Cys314=
NR_125353.1:n.1142T>C
NR_125354.1:n.1062T>C
XM_011536220.1:c.888T>C	XP_011534522.1:p.Cys296=
XM_011536221.1:c.*292T>C	XP_011534523.1:n.*292T>C
XM_011536223.1:c.306T>C	XP_011534525.1:p.Cys102=
XM_011536223.3:c.306T>C	XP_011534525.1:p.Cys102=
XR_001743705.1:n.1490T>C
NM_003880.4:c.888T>C	NP_003871.1:p.Cys296=
NM_198239.2:c.888T>C MANE Select	NP_937882.2:p.Cys296=
NR_125353.2:n.1206T>C
NR_125354.3:n.1033T>C