Canonical Allele Identifier: CA5523349
Gene: ATOH7 HGNC NCBI

Linked Data

dbSNP Id: rs771756332
ExAC: 10:69991172 T / TAGCTCAGGGCCATCTGCAGGGTCTCGTACTTGG
gnomAD v2: 10-69991172-T-TAGCTCAGGGCCATCTGCAGGGTCTCGTACTTGG
gnomAD v4: 10-68231415-T-TAGCTCAGGGCCATCTGCAGGGTCTCGTACTTGG
MyVariant Identifiers: chr10:g.69991172_69991173insAGCTCAGGGCCATCTGCAGGGTCTCGTACTTGG (hg19) chr10:g.68231415_68231416insAGCTCAGGGCCATCTGCAGGGTCTCGTACTTGG (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231417_68231449dup , CM000672.2:g.68231417_68231449dup GRCh38
NC_000010.10:g.69991174_69991206dup , CM000672.1:g.69991174_69991206dup GRCh37
NC_000010.9:g.69661180_69661212dup NCBI36
NG_031934.1:g.5666_5698dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.230_262dup MANE Select ENSP00000362777.3:p.Ser87_Tyr88insSerLysTyrGluThrLeuGlnMetAla...
ENST00000373673.4:c.230_262dup ENSP00000362777.3:p.Ser87_Tyr88insSerLysTyrGluThrLeuGlnMetAla...
NM_145178.3:c.230_262dup NP_660161.1:p.Ser87_Tyr88insSerLysTyrGluThrLeuGlnMetAlaLeuSer...
NM_145178.4:c.230_262dup MANE Select NP_660161.1:p.Ser87_Tyr88insSerLysTyrGluThrLeuGlnMetAlaLeuSer...
Search 100 bp 5'
Search 100 bp 3'