Canonical Allele Identifier: CA3963907

Gene: CCN6

Linked Data

• ClinVar Variation Id: 355058
• ClinVar RCV Id: RCV000353955 ; RCV000967008
• dbSNP Id: rs9487806
• ExAC: 6:112382223 A / T
• gnomAD v2: 6-112382223-A-T
• gnomAD v3: 6-112061020-A-T
• gnomAD v4: 6-112061020-A-T
• MyVariant Identifiers: chr6:g.112382223A>T (hg19) ; chr6:g.112061020A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112061020A>T , CM000668.2:g.112061020A>T	GRCh38
NC_000006.11:g.112382223A>T , CM000668.1:g.112382223A>T	GRCh37
NC_000006.10:g.112488916A>T	NCBI36
NG_011748.1:g.11946A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000368666.7:c.78A>T MANE Select	ENSP00000357655.4:p.Pro26=
ENST00000230529.9:c.78A>T	ENSP00000230529.5:p.Pro26=
ENST00000361714.5:c.78A>T	ENSP00000354734.2:p.Pro26=
ENST00000368663.4:c.78A>T	ENSP00000357652.4:p.Pro26=
ENST00000368664.7:c.132A>T	ENSP00000357653.3:p.Pro44=
ENST00000368666.6:c.132A>T	ENSP00000357655.3:p.Pro44=
ENST00000409166.5:c.-507-259A>T	ENSP00000386467.1:n.-507-259A>T
ENST00000454589.5:c.78A>T	ENSP00000395928.1:p.Pro26=
ENST00000604763.5:c.78A>T	ENSP00000473777.1:p.Pro26=
ENST00000620524.3:n.64-52A>T
NM_003880.3:c.78A>T	NP_003871.1:p.Pro26=
NM_198239.1:c.132A>T	NP_937882.1:p.Pro44=
NR_125353.1:n.268A>T
NR_125354.1:n.188A>T
XM_011536220.1:c.78A>T	XP_011534522.1:p.Pro26=
XM_011536221.1:c.141A>T	XP_011534523.1:p.Pro47=
XM_011536222.1:c.216A>T	XP_011534524.1:p.Pro72=
XM_011536222.2:c.141A>T	XP_011534524.2:p.Pro47=
XR_001743705.1:n.616A>T
NM_003880.4:c.78A>T	NP_003871.1:p.Pro26=
NM_198239.2:c.78A>T MANE Select	NP_937882.2:p.Pro26=
NR_125353.2:n.332A>T
NR_125354.3:n.159A>T