Canonical Allele Identifier: CA365369520

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382396A>T (hg19) ; chr6:g.112061193A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061193A>T , CM000668.2:g.112061193A>T	GRCh38
NC_000006.11:g.112382396A>T , CM000668.1:g.112382396A>T	GRCh37
NC_000006.10:g.112489089A>T	NCBI36
NG_011748.1:g.12119A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.251A>T MANE Select	ENSP00000357655.4:p.Glu84Val
ENST00000639360.1:c.155A>T	ENSP00000491774.1:p.Glu52Val
ENST00000230529.9:c.251A>T	ENSP00000230529.5:p.Glu84Val
ENST00000361714.5:c.251A>T	ENSP00000354734.2:p.Glu84Val
ENST00000368663.4:c.251A>T	ENSP00000357652.4:p.Glu84Val
ENST00000368664.7:c.305A>T	ENSP00000357653.3:p.Glu102Val
ENST00000368666.6:c.305A>T	ENSP00000357655.3:p.Glu102Val
ENST00000409166.5:c.-507-86A>T	ENSP00000386467.1:n.-507-86A>T
ENST00000454589.5:c.251A>T	ENSP00000395928.1:p.Glu84Val
ENST00000604763.5:c.251A>T	ENSP00000473777.1:p.Glu84Val
ENST00000620524.3:n.185A>T
NM_003880.3:c.251A>T	NP_003871.1:p.Glu84Val
NM_198239.1:c.305A>T	NP_937882.1:p.Glu102Val
NR_125353.1:n.441A>T
NR_125354.1:n.361A>T
XM_011536220.1:c.251A>T	XP_011534522.1:p.Glu84Val
XM_011536221.1:c.314A>T	XP_011534523.1:p.Glu105Val
XM_011536222.1:c.389A>T	XP_011534524.1:p.Glu130Val
XM_011536222.2:c.314A>T	XP_011534524.2:p.Glu105Val
XR_001743705.1:n.789A>T
NM_003880.4:c.251A>T	NP_003871.1:p.Glu84Val
NM_198239.2:c.251A>T MANE Select	NP_937882.2:p.Glu84Val
NR_125353.2:n.505A>T
NR_125354.3:n.332A>T