Canonical Allele Identifier: CA1917241638
Gene: ATOH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231606C= , CM000672.2:g.68231606C= GRCh38
NC_000010.10:g.69991363C= , CM000672.1:g.69991363C= GRCh37
NC_000010.9:g.69661369C= NCBI36
NG_031934.1:g.5508G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.72G= MANE Select ENSP00000362777.3:p.Glu24=
ENST00000373673.4:c.72G= ENSP00000362777.3:p.Glu24=
NM_145178.3:c.72G= NP_660161.1:p.Glu24=
NM_145178.4:c.72G= MANE Select NP_660161.1:p.Glu24=