Canonical Allele Identifier: CA365369461

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382387A>C (hg19) ; chr6:g.112061184A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061184A>C , CM000668.2:g.112061184A>C	GRCh38
NC_000006.11:g.112382387A>C , CM000668.1:g.112382387A>C	GRCh37
NC_000006.10:g.112489080A>C	NCBI36
NG_011748.1:g.12110A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.242A>C MANE Select	ENSP00000357655.4:p.Gln81Pro
ENST00000639360.1:c.146A>C	ENSP00000491774.1:p.Gln49Pro
ENST00000230529.9:c.242A>C	ENSP00000230529.5:p.Gln81Pro
ENST00000361714.5:c.242A>C	ENSP00000354734.2:p.Gln81Pro
ENST00000368663.4:c.242A>C	ENSP00000357652.4:p.Gln81Pro
ENST00000368664.7:c.296A>C	ENSP00000357653.3:p.Gln99Pro
ENST00000368666.6:c.296A>C	ENSP00000357655.3:p.Gln99Pro
ENST00000409166.5:c.-507-95A>C	ENSP00000386467.1:n.-507-95A>C
ENST00000454589.5:c.242A>C	ENSP00000395928.1:p.Gln81Pro
ENST00000604763.5:c.242A>C	ENSP00000473777.1:p.Gln81Pro
ENST00000620524.3:n.176A>C
NM_003880.3:c.242A>C	NP_003871.1:p.Gln81Pro
NM_198239.1:c.296A>C	NP_937882.1:p.Gln99Pro
NR_125353.1:n.432A>C
NR_125354.1:n.352A>C
XM_011536220.1:c.242A>C	XP_011534522.1:p.Gln81Pro
XM_011536221.1:c.305A>C	XP_011534523.1:p.Gln102Pro
XM_011536222.1:c.380A>C	XP_011534524.1:p.Gln127Pro
XM_011536222.2:c.305A>C	XP_011534524.2:p.Gln102Pro
XR_001743705.1:n.780A>C
NM_003880.4:c.242A>C	NP_003871.1:p.Gln81Pro
NM_198239.2:c.242A>C MANE Select	NP_937882.2:p.Gln81Pro
NR_125353.2:n.496A>C
NR_125354.3:n.323A>C