Canonical Allele Identifier: CA365368653

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382285T>A (hg19) ; chr6:g.112061082T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061082T>A , CM000668.2:g.112061082T>A	GRCh38
NC_000006.11:g.112382285T>A , CM000668.1:g.112382285T>A	GRCh37
NC_000006.10:g.112488978T>A	NCBI36
NG_011748.1:g.12008T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.140T>A MANE Select	ENSP00000357655.4:p.Phe47Tyr
ENST00000639360.1:c.44T>A	ENSP00000491774.1:p.Phe15Tyr
ENST00000230529.9:c.140T>A	ENSP00000230529.5:p.Phe47Tyr
ENST00000361714.5:c.140T>A	ENSP00000354734.2:p.Phe47Tyr
ENST00000368663.4:c.140T>A	ENSP00000357652.4:p.Phe47Tyr
ENST00000368664.7:c.194T>A	ENSP00000357653.3:p.Phe65Tyr
ENST00000368666.6:c.194T>A	ENSP00000357655.3:p.Phe65Tyr
ENST00000409166.5:c.-507-197T>A	ENSP00000386467.1:n.-507-197T>A
ENST00000454589.5:c.140T>A	ENSP00000395928.1:p.Phe47Tyr
ENST00000604763.5:c.140T>A	ENSP00000473777.1:p.Phe47Tyr
ENST00000620524.3:n.74T>A
NM_003880.3:c.140T>A	NP_003871.1:p.Phe47Tyr
NM_198239.1:c.194T>A	NP_937882.1:p.Phe65Tyr
NR_125353.1:n.330T>A
NR_125354.1:n.250T>A
XM_011536220.1:c.140T>A	XP_011534522.1:p.Phe47Tyr
XM_011536221.1:c.203T>A	XP_011534523.1:p.Phe68Tyr
XM_011536222.1:c.278T>A	XP_011534524.1:p.Phe93Tyr
XM_011536222.2:c.203T>A	XP_011534524.2:p.Phe68Tyr
XR_001743705.1:n.678T>A
NM_003880.4:c.140T>A	NP_003871.1:p.Phe47Tyr
NM_198239.2:c.140T>A MANE Select	NP_937882.2:p.Phe47Tyr
NR_125353.2:n.394T>A
NR_125354.3:n.221T>A