Canonical Allele Identifier: CA451598939

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390820G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069617G>C , CM000668.2:g.112069617G>C	GRCh38
NC_000006.11:g.112390820G>C , CM000668.1:g.112390820G>C	GRCh37
NC_000006.10:g.112497513G>C	NCBI36
NG_011748.1:g.20543G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1062G>C MANE Select	ENSP00000357655.4:p.Leu354=
ENST00000639360.1:c.963G>C	ENSP00000491774.1:p.Leu321=
ENST00000230529.9:c.1062G>C	ENSP00000230529.5:p.Leu354=
ENST00000361714.5:c.1062G>C	ENSP00000354734.2:p.Leu354=
ENST00000368663.4:c.*368G>C	ENSP00000357652.4:n.*368G>C
ENST00000368664.7:c.*466G>C	ENSP00000357653.3:n.*466G>C
ENST00000368666.6:c.1116G>C	ENSP00000357655.3:p.Leu372=
ENST00000409166.5:c.390G>C	ENSP00000386467.1:p.Leu130=
ENST00000454589.5:c.*466G>C	ENSP00000395928.1:n.*466G>C
ENST00000604763.5:c.1062G>C	ENSP00000473777.1:p.Leu354=
ENST00000613648.1:n.897G>C
ENST00000620524.3:n.993G>C
NM_003880.3:c.1062G>C	NP_003871.1:p.Leu354=
NM_198239.1:c.1116G>C	NP_937882.1:p.Leu372=
NR_125353.1:n.1316G>C
NR_125354.1:n.1236G>C
XM_011536220.1:c.1062G>C	XP_011534522.1:p.Leu354=
XM_011536221.1:c.*466G>C	XP_011534523.1:n.*466G>C
XM_011536223.1:c.480G>C	XP_011534525.1:p.Leu160=
XM_011536223.3:c.480G>C	XP_011534525.1:p.Leu160=
XR_001743705.1:n.1664G>C
NM_003880.4:c.1062G>C	NP_003871.1:p.Leu354=
NM_198239.2:c.1062G>C MANE Select	NP_937882.2:p.Leu354=
NR_125353.2:n.1380G>C
NR_125354.3:n.1207G>C