Canonical Allele Identifier: CA451901177

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382379T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061176T>C , CM000668.2:g.112061176T>C	GRCh38
NC_000006.11:g.112382379T>C , CM000668.1:g.112382379T>C	GRCh37
NC_000006.10:g.112489072T>C	NCBI36
NG_011748.1:g.12102T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.234T>C MANE Select	ENSP00000357655.4:p.Cys78=
ENST00000639360.1:c.138T>C	ENSP00000491774.1:p.Cys46=
ENST00000230529.9:c.234T>C	ENSP00000230529.5:p.Cys78=
ENST00000361714.5:c.234T>C	ENSP00000354734.2:p.Cys78=
ENST00000368663.4:c.234T>C	ENSP00000357652.4:p.Cys78=
ENST00000368664.7:c.288T>C	ENSP00000357653.3:p.Cys96=
ENST00000368666.6:c.288T>C	ENSP00000357655.3:p.Cys96=
ENST00000409166.5:c.-507-103T>C	ENSP00000386467.1:n.-507-103T>C
ENST00000454589.5:c.234T>C	ENSP00000395928.1:p.Cys78=
ENST00000604763.5:c.234T>C	ENSP00000473777.1:p.Cys78=
ENST00000620524.3:n.168T>C
NM_003880.3:c.234T>C	NP_003871.1:p.Cys78=
NM_198239.1:c.288T>C	NP_937882.1:p.Cys96=
NR_125353.1:n.424T>C
NR_125354.1:n.344T>C
XM_011536220.1:c.234T>C	XP_011534522.1:p.Cys78=
XM_011536221.1:c.297T>C	XP_011534523.1:p.Cys99=
XM_011536222.1:c.372T>C	XP_011534524.1:p.Cys124=
XM_011536222.2:c.297T>C	XP_011534524.2:p.Cys99=
XR_001743705.1:n.772T>C
NM_003880.4:c.234T>C	NP_003871.1:p.Cys78=
NM_198239.2:c.234T>C MANE Select	NP_937882.2:p.Cys78=
NR_125353.2:n.488T>C
NR_125354.3:n.315T>C