Canonical Allele Identifier: CA593850923
Gene: ATOH7 HGNC NCBI

Linked Data

gnomAD v2: 10-69991141-CT-C
gnomAD v4: 10-68231384-CT-C
MyVariant Identifiers: chr10:g.69991142del (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231385del , CM000672.2:g.68231385del GRCh38
NC_000010.10:g.69991142del , CM000672.1:g.69991142del GRCh37
NC_000010.9:g.69661148del NCBI36
NG_031934.1:g.5729del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.293del MANE Select ENSP00000362777.3:p.Glu98GlyfsTer?
ENST00000373673.4:c.293del ENSP00000362777.3:p.Glu98GlyfsTer?
NM_145178.3:c.293del NP_660161.1:p.Glu98GlyfsTer?
NM_145178.4:c.293del MANE Select NP_660161.1:p.Glu98GlyfsTer?
Search 100 bp 5'
Search 100 bp 3'