Canonical Allele Identifier: CA365367657

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382198G>C (hg19) ; chr6:g.112060995G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112060995G>C , CM000668.2:g.112060995G>C	GRCh38
NC_000006.11:g.112382198G>C , CM000668.1:g.112382198G>C	GRCh37
NC_000006.10:g.112488891G>C	NCBI36
NG_011748.1:g.11921G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.53G>C MANE Select	ENSP00000357655.4:p.Cys18Ser
ENST00000230529.9:c.53G>C	ENSP00000230529.5:p.Cys18Ser
ENST00000361714.5:c.53G>C	ENSP00000354734.2:p.Cys18Ser
ENST00000368663.4:c.53G>C	ENSP00000357652.4:p.Cys18Ser
ENST00000368664.7:c.107G>C	ENSP00000357653.3:p.Cys36Ser
ENST00000368666.6:c.107G>C	ENSP00000357655.3:p.Cys36Ser
ENST00000409166.5:c.-507-284G>C	ENSP00000386467.1:n.-507-284G>C
ENST00000454589.5:c.53G>C	ENSP00000395928.1:p.Cys18Ser
ENST00000604763.5:c.53G>C	ENSP00000473777.1:p.Cys18Ser
ENST00000620524.3:n.64-77G>C
NM_003880.3:c.53G>C	NP_003871.1:p.Cys18Ser
NM_198239.1:c.107G>C	NP_937882.1:p.Cys36Ser
NR_125353.1:n.243G>C
NR_125354.1:n.163G>C
XM_011536220.1:c.53G>C	XP_011534522.1:p.Cys18Ser
XM_011536221.1:c.116G>C	XP_011534523.1:p.Cys39Ser
XM_011536222.1:c.191G>C	XP_011534524.1:p.Cys64Ser
XM_011536222.2:c.116G>C	XP_011534524.2:p.Cys39Ser
XR_001743705.1:n.591G>C
NM_003880.4:c.53G>C	NP_003871.1:p.Cys18Ser
NM_198239.2:c.53G>C MANE Select	NP_937882.2:p.Cys18Ser
NR_125353.2:n.307G>C
NR_125354.3:n.134G>C