Canonical Allele Identifier: CA2658239278

Gene: OTOF

Linked Data

• gnomAD v4: 2-26483425-ACCCAGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26483433_26483438del , CM000664.2:g.26483433_26483438del	GRCh38
NC_000002.11:g.26706301_26706306del , CM000664.1:g.26706301_26706306del	GRCh37
NC_000002.10:g.26559805_26559810del	NCBI36
NG_009937.1:g.80268_80273del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1392+31_1392+36del MANE Select	ENSP00000272371.2:n.1392+31_1392+36del
ENST00000272371.6:c.1392+31_1392+36del	ENSP00000272371.2:n.1392+31_1392+36del
ENST00000403946.7:c.1392+31_1392+36del	ENSP00000385255.3:n.1392+31_1392+36del
NM_001287489.1:c.1392+31_1392+36del	NP_001274418.1:n.1392+31_1392+36del
NM_194248.2:c.1392+31_1392+36del	NP_919224.1:n.1392+31_1392+36del
XM_005264644.2:c.1437+31_1437+36del	XP_005264701.1:n.1437+31_1437+36del
XM_011533185.1:c.1437+31_1437+36del	XP_011531487.1:n.1437+31_1437+36del
XM_017005338.1:c.1392+31_1392+36del	XP_016860827.1:n.1392+31_1392+36del
NM_001287489.2:c.1392+31_1392+36del	NP_001274418.1:n.1392+31_1392+36del
NM_194248.3:c.1392+31_1392+36del MANE Select	NP_919224.1:n.1392+31_1392+36del