Canonical Allele Identifier: CA365367719

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382202C>A (hg19) ; chr6:g.112060999C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112060999C>A , CM000668.2:g.112060999C>A	GRCh38
NC_000006.11:g.112382202C>A , CM000668.1:g.112382202C>A	GRCh37
NC_000006.10:g.112488895C>A	NCBI36
NG_011748.1:g.11925C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.57C>A MANE Select	ENSP00000357655.4:p.Cys19Ter
ENST00000230529.9:c.57C>A	ENSP00000230529.5:p.Cys19Ter
ENST00000361714.5:c.57C>A	ENSP00000354734.2:p.Cys19Ter
ENST00000368663.4:c.57C>A	ENSP00000357652.4:p.Cys19Ter
ENST00000368664.7:c.111C>A	ENSP00000357653.3:p.Cys37Ter
ENST00000368666.6:c.111C>A	ENSP00000357655.3:p.Cys37Ter
ENST00000409166.5:c.-507-280C>A	ENSP00000386467.1:n.-507-280C>A
ENST00000454589.5:c.57C>A	ENSP00000395928.1:p.Cys19Ter
ENST00000604763.5:c.57C>A	ENSP00000473777.1:p.Cys19Ter
ENST00000620524.3:n.64-73C>A
NM_003880.3:c.57C>A	NP_003871.1:p.Cys19Ter
NM_198239.1:c.111C>A	NP_937882.1:p.Cys37Ter
NR_125353.1:n.247C>A
NR_125354.1:n.167C>A
XM_011536220.1:c.57C>A	XP_011534522.1:p.Cys19Ter
XM_011536221.1:c.120C>A	XP_011534523.1:p.Cys40Ter
XM_011536222.1:c.195C>A	XP_011534524.1:p.Cys65Ter
XM_011536222.2:c.120C>A	XP_011534524.2:p.Cys40Ter
XR_001743705.1:n.595C>A
NM_003880.4:c.57C>A	NP_003871.1:p.Cys19Ter
NM_198239.2:c.57C>A MANE Select	NP_937882.2:p.Cys19Ter
NR_125353.2:n.311C>A
NR_125354.3:n.138C>A