Canonical Allele Identifier: CA365376549

Gene: CCN6

Linked Data

• dbSNP Id: rs1583588805
• MyVariant Identifiers: chr6:g.112390741A>T (hg19) ; chr6:g.112069538A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069538A>T , CM000668.2:g.112069538A>T	GRCh38
NC_000006.11:g.112390741A>T , CM000668.1:g.112390741A>T	GRCh37
NC_000006.10:g.112497434A>T	NCBI36
NG_011748.1:g.20464A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.983A>T MANE Select	ENSP00000357655.4:p.Lys328Met
ENST00000639360.1:c.884A>T	ENSP00000491774.1:p.Lys295Met
ENST00000230529.9:c.983A>T	ENSP00000230529.5:p.Lys328Met
ENST00000361714.5:c.983A>T	ENSP00000354734.2:p.Lys328Met
ENST00000368663.4:c.*289A>T	ENSP00000357652.4:n.*289A>T
ENST00000368664.7:c.*387A>T	ENSP00000357653.3:n.*387A>T
ENST00000368666.6:c.1037A>T	ENSP00000357655.3:p.Lys346Met
ENST00000409166.5:c.311A>T	ENSP00000386467.1:p.Lys104Met
ENST00000454589.5:c.*387A>T	ENSP00000395928.1:n.*387A>T
ENST00000604763.5:c.983A>T	ENSP00000473777.1:p.Lys328Met
ENST00000613648.1:n.818A>T
ENST00000620524.3:n.914A>T
NM_003880.3:c.983A>T	NP_003871.1:p.Lys328Met
NM_198239.1:c.1037A>T	NP_937882.1:p.Lys346Met
NR_125353.1:n.1237A>T
NR_125354.1:n.1157A>T
XM_011536220.1:c.983A>T	XP_011534522.1:p.Lys328Met
XM_011536221.1:c.*387A>T	XP_011534523.1:n.*387A>T
XM_011536223.1:c.401A>T	XP_011534525.1:p.Lys134Met
XM_011536223.3:c.401A>T	XP_011534525.1:p.Lys134Met
XR_001743705.1:n.1585A>T
NM_003880.4:c.983A>T	NP_003871.1:p.Lys328Met
NM_198239.2:c.983A>T MANE Select	NP_937882.2:p.Lys328Met
NR_125353.2:n.1301A>T
NR_125354.3:n.1128A>T