Canonical Allele Identifier: CA3963933

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061139G>A , CM000668.2:g.112061139G>A	GRCh38
NC_000006.11:g.112382342G>A , CM000668.1:g.112382342G>A	GRCh37
NC_000006.10:g.112489035G>A	NCBI36
NG_011748.1:g.12065G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_198239.2:c.197G>A MANE Select	NP_937882.2:p.Ser66Asn
ENST00000368666.7:c.197G>A MANE Select	ENSP00000357655.4:p.Ser66Asn
NM_003880.3:c.197G>A	NP_003871.1:p.Ser66Asn
NM_003880.4:c.197G>A	NP_003871.1:p.Ser66Asn
NM_198239.1:c.251G>A	NP_937882.1:p.Ser84Asn
NR_125353.1:n.387G>A
NR_125353.2:n.451G>A
NR_125354.1:n.307G>A
NR_125354.3:n.278G>A
ENST00000230529.9:c.197G>A	ENSP00000230529.5:p.Ser66Asn
ENST00000361714.5:c.197G>A	ENSP00000354734.2:p.Ser66Asn
ENST00000368663.4:c.197G>A	ENSP00000357652.4:p.Ser66Asn
ENST00000368664.7:c.251G>A	ENSP00000357653.3:p.Ser84Asn
ENST00000368666.6:c.251G>A	ENSP00000357655.3:p.Ser84Asn
ENST00000409166.5:c.-507-140G>A	ENSP00000386467.1:n.-507-140G>A
ENST00000454589.5:c.197G>A	ENSP00000395928.1:p.Ser66Asn
ENST00000604763.5:c.197G>A	ENSP00000473777.1:p.Ser66Asn
ENST00000620524.3:n.131G>A
ENST00000639360.1:c.101G>A	ENSP00000491774.1:p.Ser34Asn
XM_011536220.1:c.197G>A	XP_011534522.1:p.Ser66Asn
XM_011536221.1:c.260G>A	XP_011534523.1:p.Ser87Asn
XM_011536222.1:c.335G>A	XP_011534524.1:p.Ser112Asn
XM_011536222.2:c.260G>A	XP_011534524.2:p.Ser87Asn
XR_001743705.1:n.735G>A