Canonical Allele Identifier: CA2573145337
Gene: ATOH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1351089
ClinVar RCV Id: RCV002051479
dbSNP Id: rs2134380243
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231316del , CM000672.2:g.68231316del GRCh38
NC_000010.10:g.69991073del , CM000672.1:g.69991073del GRCh37
NC_000010.9:g.69661079del NCBI36
NG_031934.1:g.5798del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.362del MANE Select ENSP00000362777.3:p.Tyr121SerfsTer?
ENST00000373673.4:c.362del ENSP00000362777.3:p.Tyr121SerfsTer?
NM_145178.3:c.362del NP_660161.1:p.Tyr121SerfsTer?
NM_145178.4:c.362del MANE Select NP_660161.1:p.Tyr121SerfsTer?
Search 100 bp 5'
Search 100 bp 3'