Canonical Allele Identifier: CA365376047

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069433-C-T
• MyVariant Identifiers: chr6:g.112390636C>T (hg19) ; chr6:g.112069433C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069433C>T , CM000668.2:g.112069433C>T	GRCh38
NC_000006.11:g.112390636C>T , CM000668.1:g.112390636C>T	GRCh37
NC_000006.10:g.112497329C>T	NCBI36
NG_011748.1:g.20359C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.878C>T MANE Select	ENSP00000357655.4:p.Pro293Leu
ENST00000639360.1:c.779C>T	ENSP00000491774.1:p.Pro260Leu
ENST00000230529.9:c.878C>T	ENSP00000230529.5:p.Pro293Leu
ENST00000361714.5:c.878C>T	ENSP00000354734.2:p.Pro293Leu
ENST00000368663.4:c.*184C>T	ENSP00000357652.4:n.*184C>T
ENST00000368664.7:c.*282C>T	ENSP00000357653.3:n.*282C>T
ENST00000368666.6:c.932C>T	ENSP00000357655.3:p.Pro311Leu
ENST00000409166.5:c.206C>T	ENSP00000386467.1:p.Pro69Leu
ENST00000454589.5:c.*282C>T	ENSP00000395928.1:n.*282C>T
ENST00000604763.5:c.878C>T	ENSP00000473777.1:p.Pro293Leu
ENST00000613648.1:n.713C>T
ENST00000620524.3:n.809C>T
NM_003880.3:c.878C>T	NP_003871.1:p.Pro293Leu
NM_198239.1:c.932C>T	NP_937882.1:p.Pro311Leu
NR_125353.1:n.1132C>T
NR_125354.1:n.1052C>T
XM_011536220.1:c.878C>T	XP_011534522.1:p.Pro293Leu
XM_011536221.1:c.*282C>T	XP_011534523.1:n.*282C>T
XM_011536223.1:c.296C>T	XP_011534525.1:p.Pro99Leu
XM_011536223.3:c.296C>T	XP_011534525.1:p.Pro99Leu
XR_001743705.1:n.1480C>T
NM_003880.4:c.878C>T	NP_003871.1:p.Pro293Leu
NM_198239.2:c.878C>T MANE Select	NP_937882.2:p.Pro293Leu
NR_125353.2:n.1196C>T
NR_125354.3:n.1023C>T