Canonical Allele Identifier: CA365367615

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382195T>G (hg19) ; chr6:g.112060992T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112060992T>G , CM000668.2:g.112060992T>G	GRCh38
NC_000006.11:g.112382195T>G , CM000668.1:g.112382195T>G	GRCh37
NC_000006.10:g.112488888T>G	NCBI36
NG_011748.1:g.11918T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.50T>G MANE Select	ENSP00000357655.4:p.Phe17Cys
ENST00000230529.9:c.50T>G	ENSP00000230529.5:p.Phe17Cys
ENST00000361714.5:c.50T>G	ENSP00000354734.2:p.Phe17Cys
ENST00000368663.4:c.50T>G	ENSP00000357652.4:p.Phe17Cys
ENST00000368664.7:c.104T>G	ENSP00000357653.3:p.Phe35Cys
ENST00000368666.6:c.104T>G	ENSP00000357655.3:p.Phe35Cys
ENST00000409166.5:c.-507-287T>G	ENSP00000386467.1:n.-507-287T>G
ENST00000454589.5:c.50T>G	ENSP00000395928.1:p.Phe17Cys
ENST00000604763.5:c.50T>G	ENSP00000473777.1:p.Phe17Cys
ENST00000620524.3:n.64-80T>G
NM_003880.3:c.50T>G	NP_003871.1:p.Phe17Cys
NM_198239.1:c.104T>G	NP_937882.1:p.Phe35Cys
NR_125353.1:n.240T>G
NR_125354.1:n.160T>G
XM_011536220.1:c.50T>G	XP_011534522.1:p.Phe17Cys
XM_011536221.1:c.113T>G	XP_011534523.1:p.Phe38Cys
XM_011536222.1:c.188T>G	XP_011534524.1:p.Phe63Cys
XM_011536222.2:c.113T>G	XP_011534524.2:p.Phe38Cys
XR_001743705.1:n.588T>G
NM_003880.4:c.50T>G	NP_003871.1:p.Phe17Cys
NM_198239.2:c.50T>G MANE Select	NP_937882.2:p.Phe17Cys
NR_125353.2:n.304T>G
NR_125354.3:n.131T>G