Canonical Allele Identifier: CA144880770

Gene: CCN6

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061091G>A , CM000668.2:g.112061091G>A	GRCh38
NC_000006.11:g.112382294G>A , CM000668.1:g.112382294G>A	GRCh37
NC_000006.10:g.112488987G>A	NCBI36
NG_011748.1:g.12017G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_198239.2:c.149G>A MANE Select	NP_937882.2:p.Trp50Ter
ENST00000368666.7:c.149G>A MANE Select	ENSP00000357655.4:p.Trp50Ter
NM_003880.3:c.149G>A	NP_003871.1:p.Trp50Ter
NM_003880.4:c.149G>A	NP_003871.1:p.Trp50Ter
NM_198239.1:c.203G>A	NP_937882.1:p.Trp68Ter
NR_125353.1:n.339G>A
NR_125353.2:n.403G>A
NR_125354.1:n.259G>A
NR_125354.3:n.230G>A
ENST00000230529.9:c.149G>A	ENSP00000230529.5:p.Trp50Ter
ENST00000361714.5:c.149G>A	ENSP00000354734.2:p.Trp50Ter
ENST00000368663.4:c.149G>A	ENSP00000357652.4:p.Trp50Ter
ENST00000368664.7:c.203G>A	ENSP00000357653.3:p.Trp68Ter
ENST00000368666.6:c.203G>A	ENSP00000357655.3:p.Trp68Ter
ENST00000409166.5:c.-507-188G>A	ENSP00000386467.1:n.-507-188G>A
ENST00000454589.5:c.149G>A	ENSP00000395928.1:p.Trp50Ter
ENST00000604763.5:c.149G>A	ENSP00000473777.1:p.Trp50Ter
ENST00000620524.3:n.83G>A
ENST00000639360.1:c.53G>A	ENSP00000491774.1:p.Trp18Ter
XM_011536220.1:c.149G>A	XP_011534522.1:p.Trp50Ter
XM_011536221.1:c.212G>A	XP_011534523.1:p.Trp71Ter
XM_011536222.1:c.287G>A	XP_011534524.1:p.Trp96Ter
XM_011536222.2:c.212G>A	XP_011534524.2:p.Trp71Ter
XR_001743705.1:n.687G>A