Canonical Allele Identifier: CA365369473

Gene: CCN6

Linked Data

• MyVariant Identifiers: chr6:g.112382389C>G (hg19) ; chr6:g.112061186C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061186C>G , CM000668.2:g.112061186C>G	GRCh38
NC_000006.11:g.112382389C>G , CM000668.1:g.112382389C>G	GRCh37
NC_000006.10:g.112489082C>G	NCBI36
NG_011748.1:g.12112C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.244C>G MANE Select	ENSP00000357655.4:p.Pro82Ala
ENST00000639360.1:c.148C>G	ENSP00000491774.1:p.Pro50Ala
ENST00000230529.9:c.244C>G	ENSP00000230529.5:p.Pro82Ala
ENST00000361714.5:c.244C>G	ENSP00000354734.2:p.Pro82Ala
ENST00000368663.4:c.244C>G	ENSP00000357652.4:p.Pro82Ala
ENST00000368664.7:c.298C>G	ENSP00000357653.3:p.Pro100Ala
ENST00000368666.6:c.298C>G	ENSP00000357655.3:p.Pro100Ala
ENST00000409166.5:c.-507-93C>G	ENSP00000386467.1:n.-507-93C>G
ENST00000454589.5:c.244C>G	ENSP00000395928.1:p.Pro82Ala
ENST00000604763.5:c.244C>G	ENSP00000473777.1:p.Pro82Ala
ENST00000620524.3:n.178C>G
NM_003880.3:c.244C>G	NP_003871.1:p.Pro82Ala
NM_198239.1:c.298C>G	NP_937882.1:p.Pro100Ala
NR_125353.1:n.434C>G
NR_125354.1:n.354C>G
XM_011536220.1:c.244C>G	XP_011534522.1:p.Pro82Ala
XM_011536221.1:c.307C>G	XP_011534523.1:p.Pro103Ala
XM_011536222.1:c.382C>G	XP_011534524.1:p.Pro128Ala
XM_011536222.2:c.307C>G	XP_011534524.2:p.Pro103Ala
XR_001743705.1:n.782C>G
NM_003880.4:c.244C>G	NP_003871.1:p.Pro82Ala
NM_198239.2:c.244C>G MANE Select	NP_937882.2:p.Pro82Ala
NR_125353.2:n.498C>G
NR_125354.3:n.325C>G