Canonical Allele Identifier: CA2680045422

Gene: CCN6

Linked Data

• gnomAD v4: 6-112069652-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.112069652C>T , CM000668.2:g.112069652C>T	GRCh38
NC_000006.11:g.112390855C>T , CM000668.1:g.112390855C>T	GRCh37
NC_000006.10:g.112497548C>T	NCBI36
NG_011748.1:g.20578C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000368666.7:c.*32C>T MANE Select	ENSP00000357655.4:n.*32C>T
ENST00000639360.1:c.998C>T	ENSP00000491774.1:n.998C>T
ENST00000230529.9:c.*32C>T	ENSP00000230529.5:n.*32C>T
ENST00000361714.5:c.*32C>T	ENSP00000354734.2:n.*32C>T
ENST00000368664.7:c.*501C>T	ENSP00000357653.3:n.*501C>T
ENST00000368666.6:c.*32C>T	ENSP00000357655.3:n.*32C>T
ENST00000409166.5:c.*32C>T	ENSP00000386467.1:n.*32C>T
ENST00000454589.5:c.*501C>T	ENSP00000395928.1:n.*501C>T
ENST00000604763.5:c.*32C>T	ENSP00000473777.1:n.*32C>T
ENST00000613648.1:n.932C>T
ENST00000620524.3:n.1028C>T
NM_003880.3:c.*32C>T	NP_003871.1:n.*32C>T
NM_198239.1:c.*32C>T	NP_937882.1:n.*32C>T
NR_125353.1:n.1351C>T
NR_125354.1:n.1271C>T
XM_011536220.1:c.*32C>T	XP_011534522.1:n.*32C>T
XM_011536221.1:c.*501C>T	XP_011534523.1:n.*501C>T
XM_011536223.1:c.*32C>T	XP_011534525.1:n.*32C>T
XM_011536223.3:c.*32C>T	XP_011534525.1:n.*32C>T
XR_001743705.1:n.1699C>T
NM_003880.4:c.*32C>T	NP_003871.1:n.*32C>T
NM_198239.2:c.*32C>T MANE Select	NP_937882.2:n.*32C>T
NR_125353.2:n.1415C>T
NR_125354.3:n.1242C>T