Canonical Allele Identifier: CA365376961

Gene: CCN6

Linked Data

• dbSNP Id: rs1279000757
• MyVariant Identifiers: chr6:g.112390789C>A (hg19) ; chr6:g.112069586C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069586C>A , CM000668.2:g.112069586C>A	GRCh38
NC_000006.11:g.112390789C>A , CM000668.1:g.112390789C>A	GRCh37
NC_000006.10:g.112497482C>A	NCBI36
NG_011748.1:g.20512C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.1031C>A MANE Select	ENSP00000357655.4:p.Pro344His
ENST00000639360.1:c.932C>A	ENSP00000491774.1:p.Pro311His
ENST00000230529.9:c.1031C>A	ENSP00000230529.5:p.Pro344His
ENST00000361714.5:c.1031C>A	ENSP00000354734.2:p.Pro344His
ENST00000368663.4:c.*337C>A	ENSP00000357652.4:n.*337C>A
ENST00000368664.7:c.*435C>A	ENSP00000357653.3:n.*435C>A
ENST00000368666.6:c.1085C>A	ENSP00000357655.3:p.Pro362His
ENST00000409166.5:c.359C>A	ENSP00000386467.1:p.Pro120His
ENST00000454589.5:c.*435C>A	ENSP00000395928.1:n.*435C>A
ENST00000604763.5:c.1031C>A	ENSP00000473777.1:p.Pro344His
ENST00000613648.1:n.866C>A
ENST00000620524.3:n.962C>A
NM_003880.3:c.1031C>A	NP_003871.1:p.Pro344His
NM_198239.1:c.1085C>A	NP_937882.1:p.Pro362His
NR_125353.1:n.1285C>A
NR_125354.1:n.1205C>A
XM_011536220.1:c.1031C>A	XP_011534522.1:p.Pro344His
XM_011536221.1:c.*435C>A	XP_011534523.1:n.*435C>A
XM_011536223.1:c.449C>A	XP_011534525.1:p.Pro150His
XM_011536223.3:c.449C>A	XP_011534525.1:p.Pro150His
XR_001743705.1:n.1633C>A
NM_003880.4:c.1031C>A	NP_003871.1:p.Pro344His
NM_198239.2:c.1031C>A MANE Select	NP_937882.2:p.Pro344His
NR_125353.2:n.1349C>A
NR_125354.3:n.1176C>A