Canonical Allele Identifier: CA1917241658
Gene: ATOH7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.68231649G= , CM000672.2:g.68231649G= GRCh38
NC_000010.10:g.69991406G= , CM000672.1:g.69991406G= GRCh37
NC_000010.9:g.69661412G= NCBI36
NG_031934.1:g.5465C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000373673.5:c.29C= MANE Select ENSP00000362777.3:p.Pro10=
ENST00000373673.4:c.29C= ENSP00000362777.3:p.Pro10=
NM_145178.3:c.29C= NP_660161.1:p.Pro10=
NM_145178.4:c.29C= MANE Select NP_660161.1:p.Pro10=