Canonical Allele Identifier: CA365376675

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390755A>C (hg19) ; chr6:g.112069552A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069552A>C , CM000668.2:g.112069552A>C	GRCh38
NC_000006.11:g.112390755A>C , CM000668.1:g.112390755A>C	GRCh37
NC_000006.10:g.112497448A>C	NCBI36
NG_011748.1:g.20478A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.997A>C MANE Select	ENSP00000357655.4:p.Thr333Pro
ENST00000639360.1:c.898A>C	ENSP00000491774.1:p.Thr300Pro
ENST00000230529.9:c.997A>C	ENSP00000230529.5:p.Thr333Pro
ENST00000361714.5:c.997A>C	ENSP00000354734.2:p.Thr333Pro
ENST00000368663.4:c.*303A>C	ENSP00000357652.4:n.*303A>C
ENST00000368664.7:c.*401A>C	ENSP00000357653.3:n.*401A>C
ENST00000368666.6:c.1051A>C	ENSP00000357655.3:p.Thr351Pro
ENST00000409166.5:c.325A>C	ENSP00000386467.1:p.Thr109Pro
ENST00000454589.5:c.*401A>C	ENSP00000395928.1:n.*401A>C
ENST00000604763.5:c.997A>C	ENSP00000473777.1:p.Thr333Pro
ENST00000613648.1:n.832A>C
ENST00000620524.3:n.928A>C
NM_003880.3:c.997A>C	NP_003871.1:p.Thr333Pro
NM_198239.1:c.1051A>C	NP_937882.1:p.Thr351Pro
NR_125353.1:n.1251A>C
NR_125354.1:n.1171A>C
XM_011536220.1:c.997A>C	XP_011534522.1:p.Thr333Pro
XM_011536221.1:c.*401A>C	XP_011534523.1:n.*401A>C
XM_011536223.1:c.415A>C	XP_011534525.1:p.Thr139Pro
XM_011536223.3:c.415A>C	XP_011534525.1:p.Thr139Pro
XR_001743705.1:n.1599A>C
NM_003880.4:c.997A>C	NP_003871.1:p.Thr333Pro
NM_198239.2:c.997A>C MANE Select	NP_937882.2:p.Thr333Pro
NR_125353.2:n.1315A>C
NR_125354.3:n.1142A>C