Canonical Allele Identifier: CA593850969
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 851114
ClinVar RCV Id: RCV001055441
dbSNP Id: rs556912362
gnomAD v2: 10-69991353-T-TGCCCGCGCACTCGGTGCC
gnomAD v3: 10-68231596-T-TGCCCGCGCACTCGGTGCC
gnomAD v4: 10-68231596-T-TGCCCGCGCACTCGGTGCC
MyVariant Identifiers: chr10:g.69991371_69991372insGCCCGCGCACTCGGTGCC (hg19) chr10:g.69991353_69991354insGCCCGCGCACTCGGTGCC (hg19) chr10:g.68231614_68231615insGCCCGCGCACTCGGTGCC (hg38) chr10:g.68231596_68231597insGCCCGCGCACTCGGTGCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231607_68231624dup , CM000672.2:g.68231607_68231624dup GRCh38
NC_000010.10:g.69991364_69991381dup , CM000672.1:g.69991364_69991381dup GRCh37
NC_000010.9:g.69661370_69661387dup NCBI36
NG_031934.1:g.5500_5517dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.64_81dup MANE Select ENSP00000362777.3:p.Gly27_Thr28insGlyThrGluCysAlaGly
ENST00000373673.4:c.64_81dup ENSP00000362777.3:p.Gly27_Thr28insGlyThrGluCysAlaGly
NM_145178.3:c.64_81dup NP_660161.1:p.Gly27_Thr28insGlyThrGluCysAlaGly
NM_145178.4:c.64_81dup MANE Select NP_660161.1:p.Gly27_Thr28insGlyThrGluCysAlaGly
Search 100 bp 5'
Search 100 bp 3'