Canonical Allele Identifier: CA365369385

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382377T>G (hg19) ; chr6:g.112061174T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061174T>G , CM000668.2:g.112061174T>G	GRCh38
NC_000006.11:g.112382377T>G , CM000668.1:g.112382377T>G	GRCh37
NC_000006.10:g.112489070T>G	NCBI36
NG_011748.1:g.12100T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.232T>G MANE Select	ENSP00000357655.4:p.Cys78Gly
ENST00000639360.1:c.136T>G	ENSP00000491774.1:p.Cys46Gly
ENST00000230529.9:c.232T>G	ENSP00000230529.5:p.Cys78Gly
ENST00000361714.5:c.232T>G	ENSP00000354734.2:p.Cys78Gly
ENST00000368663.4:c.232T>G	ENSP00000357652.4:p.Cys78Gly
ENST00000368664.7:c.286T>G	ENSP00000357653.3:p.Cys96Gly
ENST00000368666.6:c.286T>G	ENSP00000357655.3:p.Cys96Gly
ENST00000409166.5:c.-507-105T>G	ENSP00000386467.1:n.-507-105T>G
ENST00000454589.5:c.232T>G	ENSP00000395928.1:p.Cys78Gly
ENST00000604763.5:c.232T>G	ENSP00000473777.1:p.Cys78Gly
ENST00000620524.3:n.166T>G
NM_003880.3:c.232T>G	NP_003871.1:p.Cys78Gly
NM_198239.1:c.286T>G	NP_937882.1:p.Cys96Gly
NR_125353.1:n.422T>G
NR_125354.1:n.342T>G
XM_011536220.1:c.232T>G	XP_011534522.1:p.Cys78Gly
XM_011536221.1:c.295T>G	XP_011534523.1:p.Cys99Gly
XM_011536222.1:c.370T>G	XP_011534524.1:p.Cys124Gly
XM_011536222.2:c.295T>G	XP_011534524.2:p.Cys99Gly
XR_001743705.1:n.770T>G
NM_003880.4:c.232T>G	NP_003871.1:p.Cys78Gly
NM_198239.2:c.232T>G MANE Select	NP_937882.2:p.Cys78Gly
NR_125353.2:n.486T>G
NR_125354.3:n.313T>G