Canonical Allele Identifier: CA469801204
Gene: ATOH7 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.69991341del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231587del , CM000672.2:g.68231587del GRCh38
NC_000010.10:g.69991344del , CM000672.1:g.69991344del GRCh37
NC_000010.9:g.69661350del NCBI36
NG_031934.1:g.5530del

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.94del MANE Select ENSP00000362777.3:p.Ala32ProfsTer?
ENST00000373673.4:c.94del ENSP00000362777.3:p.Ala32ProfsTer?
NM_145178.3:c.94del NP_660161.1:p.Ala32ProfsTer?
NM_145178.4:c.94del MANE Select NP_660161.1:p.Ala32ProfsTer?