Canonical Allele Identifier: CA451901426

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112390754T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069551T>A , CM000668.2:g.112069551T>A	GRCh38
NC_000006.11:g.112390754T>A , CM000668.1:g.112390754T>A	GRCh37
NC_000006.10:g.112497447T>A	NCBI36
NG_011748.1:g.20477T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.996T>A MANE Select	ENSP00000357655.4:p.Ile332=
ENST00000639360.1:c.897T>A	ENSP00000491774.1:p.Ile299=
ENST00000230529.9:c.996T>A	ENSP00000230529.5:p.Ile332=
ENST00000361714.5:c.996T>A	ENSP00000354734.2:p.Ile332=
ENST00000368663.4:c.*302T>A	ENSP00000357652.4:n.*302T>A
ENST00000368664.7:c.*400T>A	ENSP00000357653.3:n.*400T>A
ENST00000368666.6:c.1050T>A	ENSP00000357655.3:p.Ile350=
ENST00000409166.5:c.324T>A	ENSP00000386467.1:p.Ile108=
ENST00000454589.5:c.*400T>A	ENSP00000395928.1:n.*400T>A
ENST00000604763.5:c.996T>A	ENSP00000473777.1:p.Ile332=
ENST00000613648.1:n.831T>A
ENST00000620524.3:n.927T>A
NM_003880.3:c.996T>A	NP_003871.1:p.Ile332=
NM_198239.1:c.1050T>A	NP_937882.1:p.Ile350=
NR_125353.1:n.1250T>A
NR_125354.1:n.1170T>A
XM_011536220.1:c.996T>A	XP_011534522.1:p.Ile332=
XM_011536221.1:c.*400T>A	XP_011534523.1:n.*400T>A
XM_011536223.1:c.414T>A	XP_011534525.1:p.Ile138=
XM_011536223.3:c.414T>A	XP_011534525.1:p.Ile138=
XR_001743705.1:n.1598T>A
NM_003880.4:c.996T>A	NP_003871.1:p.Ile332=
NM_198239.2:c.996T>A MANE Select	NP_937882.2:p.Ile332=
NR_125353.2:n.1314T>A
NR_125354.3:n.1141T>A