Canonical Allele Identifier: CA365368968

Gene: CCN6

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061120C>A , CM000668.2:g.112061120C>A	GRCh38
NC_000006.11:g.112382323C>A , CM000668.1:g.112382323C>A	GRCh37
NC_000006.10:g.112489016C>A	NCBI36
NG_011748.1:g.12046C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.178C>A MANE Select	ENSP00000357655.4:p.Arg60Ser
ENST00000639360.1:c.82C>A	ENSP00000491774.1:p.Arg28Ser
ENST00000230529.9:c.178C>A	ENSP00000230529.5:p.Arg60Ser
ENST00000361714.5:c.178C>A	ENSP00000354734.2:p.Arg60Ser
ENST00000368663.4:c.178C>A	ENSP00000357652.4:p.Arg60Ser
ENST00000368664.7:c.232C>A	ENSP00000357653.3:p.Arg78Ser
ENST00000368666.6:c.232C>A	ENSP00000357655.3:p.Arg78Ser
ENST00000409166.5:c.-507-159C>A	ENSP00000386467.1:n.-507-159C>A
ENST00000454589.5:c.178C>A	ENSP00000395928.1:p.Arg60Ser
ENST00000604763.5:c.178C>A	ENSP00000473777.1:p.Arg60Ser
ENST00000620524.3:n.112C>A
NM_003880.3:c.178C>A	NP_003871.1:p.Arg60Ser
NM_198239.1:c.232C>A	NP_937882.1:p.Arg78Ser
NR_125353.1:n.368C>A
NR_125354.1:n.288C>A
XM_011536220.1:c.178C>A	XP_011534522.1:p.Arg60Ser
XM_011536221.1:c.241C>A	XP_011534523.1:p.Arg81Ser
XM_011536222.1:c.316C>A	XP_011534524.1:p.Arg106Ser
XM_011536222.2:c.241C>A	XP_011534524.2:p.Arg81Ser
XR_001743705.1:n.716C>A
NM_003880.4:c.178C>A	NP_003871.1:p.Arg60Ser
NM_198239.2:c.178C>A MANE Select	NP_937882.2:p.Arg60Ser
NR_125353.2:n.432C>A
NR_125354.3:n.259C>A