Canonical Allele Identifier: CA451900887

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382277T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061074T>A , CM000668.2:g.112061074T>A	GRCh38
NC_000006.11:g.112382277T>A , CM000668.1:g.112382277T>A	GRCh37
NC_000006.10:g.112488970T>A	NCBI36
NG_011748.1:g.12000T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.132T>A MANE Select	ENSP00000357655.4:p.Arg44=
ENST00000639360.1:c.36T>A	ENSP00000491774.1:p.Arg12=
ENST00000230529.9:c.132T>A	ENSP00000230529.5:p.Arg44=
ENST00000361714.5:c.132T>A	ENSP00000354734.2:p.Arg44=
ENST00000368663.4:c.132T>A	ENSP00000357652.4:p.Arg44=
ENST00000368664.7:c.186T>A	ENSP00000357653.3:p.Arg62=
ENST00000368666.6:c.186T>A	ENSP00000357655.3:p.Arg62=
ENST00000409166.5:c.-507-205T>A	ENSP00000386467.1:n.-507-205T>A
ENST00000454589.5:c.132T>A	ENSP00000395928.1:p.Arg44=
ENST00000604763.5:c.132T>A	ENSP00000473777.1:p.Arg44=
ENST00000620524.3:n.66T>A
NM_003880.3:c.132T>A	NP_003871.1:p.Arg44=
NM_198239.1:c.186T>A	NP_937882.1:p.Arg62=
NR_125353.1:n.322T>A
NR_125354.1:n.242T>A
XM_011536220.1:c.132T>A	XP_011534522.1:p.Arg44=
XM_011536221.1:c.195T>A	XP_011534523.1:p.Arg65=
XM_011536222.1:c.270T>A	XP_011534524.1:p.Arg90=
XM_011536222.2:c.195T>A	XP_011534524.2:p.Arg65=
XR_001743705.1:n.670T>A
NM_003880.4:c.132T>A	NP_003871.1:p.Arg44=
NM_198239.2:c.132T>A MANE Select	NP_937882.2:p.Arg44=
NR_125353.2:n.386T>A
NR_125354.3:n.213T>A