Canonical Allele Identifier: CA365367696

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382200T>C (hg19) ; chr6:g.112060997T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112060997T>C , CM000668.2:g.112060997T>C	GRCh38
NC_000006.11:g.112382200T>C , CM000668.1:g.112382200T>C	GRCh37
NC_000006.10:g.112488893T>C	NCBI36
NG_011748.1:g.11923T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.55T>C MANE Select	ENSP00000357655.4:p.Cys19Arg
ENST00000230529.9:c.55T>C	ENSP00000230529.5:p.Cys19Arg
ENST00000361714.5:c.55T>C	ENSP00000354734.2:p.Cys19Arg
ENST00000368663.4:c.55T>C	ENSP00000357652.4:p.Cys19Arg
ENST00000368664.7:c.109T>C	ENSP00000357653.3:p.Cys37Arg
ENST00000368666.6:c.109T>C	ENSP00000357655.3:p.Cys37Arg
ENST00000409166.5:c.-507-282T>C	ENSP00000386467.1:n.-507-282T>C
ENST00000454589.5:c.55T>C	ENSP00000395928.1:p.Cys19Arg
ENST00000604763.5:c.55T>C	ENSP00000473777.1:p.Cys19Arg
ENST00000620524.3:n.64-75T>C
NM_003880.3:c.55T>C	NP_003871.1:p.Cys19Arg
NM_198239.1:c.109T>C	NP_937882.1:p.Cys37Arg
NR_125353.1:n.245T>C
NR_125354.1:n.165T>C
XM_011536220.1:c.55T>C	XP_011534522.1:p.Cys19Arg
XM_011536221.1:c.118T>C	XP_011534523.1:p.Cys40Arg
XM_011536222.1:c.193T>C	XP_011534524.1:p.Cys65Arg
XM_011536222.2:c.118T>C	XP_011534524.2:p.Cys40Arg
XR_001743705.1:n.593T>C
NM_003880.4:c.55T>C	NP_003871.1:p.Cys19Arg
NM_198239.2:c.55T>C MANE Select	NP_937882.2:p.Cys19Arg
NR_125353.2:n.309T>C
NR_125354.3:n.136T>C