Canonical Allele Identifier: CA1239831423

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26484590_26484591delinsAT , CM000664.2:g.26484590_26484591delinsAT	GRCh38
NC_000002.11:g.26707458_26707459delinsAT , CM000664.1:g.26707458_26707459delinsAT	GRCh37
NC_000002.10:g.26560962_26560963delinsAT	NCBI36
NG_009937.1:g.79108_79109delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1088_1089delinsAT MANE Select	ENSP00000272371.2:p.Asp363=
ENST00000272371.6:c.1088_1089delinsAT	ENSP00000272371.2:p.Asp363=
ENST00000403946.7:c.1088_1089delinsAT	ENSP00000385255.3:p.Asp363=
NM_001287489.1:c.1088_1089delinsAT	NP_001274418.1:p.Asp363=
NM_194248.2:c.1088_1089delinsAT	NP_919224.1:p.Asp363=
XM_005264644.2:c.1133_1134delinsAT	XP_005264701.1:p.Asp378=
XM_011533185.1:c.1133_1134delinsAT	XP_011531487.1:p.Asp378=
XM_017005338.1:c.1088_1089delinsAT	XP_016860827.1:p.Asp363=
NM_001287489.2:c.1088_1089delinsAT	NP_001274418.1:p.Asp363=
NM_194248.3:c.1088_1089delinsAT MANE Select	NP_919224.1:p.Asp363=