Canonical Allele Identifier: CA365376039

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390635C>A (hg19) ; chr6:g.112069432C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069432C>A , CM000668.2:g.112069432C>A	GRCh38
NC_000006.11:g.112390635C>A , CM000668.1:g.112390635C>A	GRCh37
NC_000006.10:g.112497328C>A	NCBI36
NG_011748.1:g.20358C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.877C>A MANE Select	ENSP00000357655.4:p.Pro293Thr
ENST00000639360.1:c.778C>A	ENSP00000491774.1:p.Pro260Thr
ENST00000230529.9:c.877C>A	ENSP00000230529.5:p.Pro293Thr
ENST00000361714.5:c.877C>A	ENSP00000354734.2:p.Pro293Thr
ENST00000368663.4:c.*183C>A	ENSP00000357652.4:n.*183C>A
ENST00000368664.7:c.*281C>A	ENSP00000357653.3:n.*281C>A
ENST00000368666.6:c.931C>A	ENSP00000357655.3:p.Pro311Thr
ENST00000409166.5:c.205C>A	ENSP00000386467.1:p.Pro69Thr
ENST00000454589.5:c.*281C>A	ENSP00000395928.1:n.*281C>A
ENST00000604763.5:c.877C>A	ENSP00000473777.1:p.Pro293Thr
ENST00000613648.1:n.712C>A
ENST00000620524.3:n.808C>A
NM_003880.3:c.877C>A	NP_003871.1:p.Pro293Thr
NM_198239.1:c.931C>A	NP_937882.1:p.Pro311Thr
NR_125353.1:n.1131C>A
NR_125354.1:n.1051C>A
XM_011536220.1:c.877C>A	XP_011534522.1:p.Pro293Thr
XM_011536221.1:c.*281C>A	XP_011534523.1:n.*281C>A
XM_011536223.1:c.295C>A	XP_011534525.1:p.Pro99Thr
XM_011536223.3:c.295C>A	XP_011534525.1:p.Pro99Thr
XR_001743705.1:n.1479C>A
NM_003880.4:c.877C>A	NP_003871.1:p.Pro293Thr
NM_198239.2:c.877C>A MANE Select	NP_937882.2:p.Pro293Thr
NR_125353.2:n.1195C>A
NR_125354.3:n.1022C>A