Canonical Allele Identifier: CA1239828679

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482206_26482211delinsTCAGGC , CM000664.2:g.26482206_26482211delinsTCAGGC	GRCh38
NC_000002.11:g.26705074_26705079delinsTCAGGC , CM000664.1:g.26705074_26705079delinsTCAGGC	GRCh37
NC_000002.10:g.26558578_26558583delinsTCAGGC	NCBI36
NG_009937.1:g.81488_81493delinsGCCTGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1579+195_1579+200delinsGCCTGA MANE Select	ENSP00000272371.2:n.1579+195_1579+200delinsGCCTGA
ENST00000272371.6:c.1579+195_1579+200delinsGCCTGA	ENSP00000272371.2:n.1579+195_1579+200delinsGCCTGA
ENST00000403946.7:c.1579+195_1579+200delinsGCCTGA	ENSP00000385255.3:n.1579+195_1579+200delinsGCCTGA
NM_001287489.1:c.1579+195_1579+200delinsGCCTGA	NP_001274418.1:n.1579+195_1579+200delinsGCCTGA
NM_194248.2:c.1579+195_1579+200delinsGCCTGA	NP_919224.1:n.1579+195_1579+200delinsGCCTGA
XM_005264644.2:c.1624+195_1624+200delinsGCCTGA	XP_005264701.1:n.1624+195_1624+200delinsGCCTGA
XM_011533185.1:c.1624+195_1624+200delinsGCCTGA	XP_011531487.1:n.1624+195_1624+200delinsGCCTGA
XM_017005338.1:c.1579+195_1579+200delinsGCCTGA	XP_016860827.1:n.1579+195_1579+200delinsGCCTGA
NM_001287489.2:c.1579+195_1579+200delinsGCCTGA	NP_001274418.1:n.1579+195_1579+200delinsGCCTGA
NM_194248.3:c.1579+195_1579+200delinsGCCTGA MANE Select	NP_919224.1:n.1579+195_1579+200delinsGCCTGA