Canonical Allele Identifier: CA1655201653
Gene: CCN6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.112069701_112069705delinsCTTTG , CM000668.2:g.112069701_112069705delinsCTTTG GRCh38
NC_000006.11:g.112390904_112390908delinsCTTTG , CM000668.1:g.112390904_112390908delinsCTTTG GRCh37
NC_000006.10:g.112497597_112497601delinsCTTTG NCBI36
NG_011748.1:g.20627_20631delinsCTTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000361714.5:c.*81_*85delinsCTTTG ENSP00000354734.2:n.*81_*85delinsCTTTG
ENST00000368666.6:c.*81_*85delinsCTTTG ENSP00000357655.3:n.*81_*85delinsCTTTG