Canonical Allele Identifier: CA365376635
Gene: CCN6 HGNC NCBI

Linked Data

gnomAD v4: 6-112069547-G-A
MyVariant Identifiers: chr6:g.112390750G>A (hg19) chr6:g.112069547G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069547G>A , CM000668.2:g.112069547G>A GRCh38
NC_000006.11:g.112390750G>A , CM000668.1:g.112390750G>A GRCh37
NC_000006.10:g.112497443G>A NCBI36
NG_011748.1:g.20473G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000368666.7:c.992G>A MANE Select ENSP00000357655.4:p.Trp331Ter
ENST00000639360.1:c.893G>A ENSP00000491774.1:p.Trp298Ter
ENST00000230529.9:c.992G>A ENSP00000230529.5:p.Trp331Ter
ENST00000361714.5:c.992G>A ENSP00000354734.2:p.Trp331Ter
ENST00000368663.4:c.*298G>A ENSP00000357652.4:n.*298G>A
ENST00000368664.7:c.*396G>A ENSP00000357653.3:n.*396G>A
ENST00000368666.6:c.1046G>A ENSP00000357655.3:p.Trp349Ter
ENST00000409166.5:c.320G>A ENSP00000386467.1:p.Trp107Ter
ENST00000454589.5:c.*396G>A ENSP00000395928.1:n.*396G>A
ENST00000604763.5:c.992G>A ENSP00000473777.1:p.Trp331Ter
ENST00000613648.1:n.827G>A
ENST00000620524.3:n.923G>A
NM_003880.3:c.992G>A NP_003871.1:p.Trp331Ter
NM_198239.1:c.1046G>A NP_937882.1:p.Trp349Ter
NR_125353.1:n.1246G>A
NR_125354.1:n.1166G>A
XM_011536220.1:c.992G>A XP_011534522.1:p.Trp331Ter
XM_011536221.1:c.*396G>A XP_011534523.1:n.*396G>A
XM_011536223.1:c.410G>A XP_011534525.1:p.Trp137Ter
XM_011536223.3:c.410G>A XP_011534525.1:p.Trp137Ter
XR_001743705.1:n.1594G>A
NM_003880.4:c.992G>A NP_003871.1:p.Trp331Ter
NM_198239.2:c.992G>A MANE Select NP_937882.2:p.Trp331Ter
NR_125353.2:n.1310G>A
NR_125354.3:n.1137G>A
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