Canonical Allele Identifier: CA1028610490

Gene: OTOF

Linked Data

• gnomAD v3: 2-26482762-TGTGTGAGTGGGTGC-T
• gnomAD v4: 2-26482762-TGTGTGAGTGGGTGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482764_26482777del , CM000664.2:g.26482764_26482777del	GRCh38
NC_000002.11:g.26705632_26705645del , CM000664.1:g.26705632_26705645del	GRCh37
NC_000002.10:g.26559136_26559149del	NCBI36
NG_009937.1:g.80923_80936del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-184_1393-171del MANE Select	ENSP00000272371.2:n.1393-184_1393-171del
ENST00000272371.6:c.1393-184_1393-171del	ENSP00000272371.2:n.1393-184_1393-171del
ENST00000403946.7:c.1393-184_1393-171del	ENSP00000385255.3:n.1393-184_1393-171del
NM_001287489.1:c.1393-184_1393-171del	NP_001274418.1:n.1393-184_1393-171del
NM_194248.2:c.1393-184_1393-171del	NP_919224.1:n.1393-184_1393-171del
XM_005264644.2:c.1438-184_1438-171del	XP_005264701.1:n.1438-184_1438-171del
XM_011533185.1:c.1438-184_1438-171del	XP_011531487.1:n.1438-184_1438-171del
XM_017005338.1:c.1393-184_1393-171del	XP_016860827.1:n.1393-184_1393-171del
NM_001287489.2:c.1393-184_1393-171del	NP_001274418.1:n.1393-184_1393-171del
NM_194248.3:c.1393-184_1393-171del MANE Select	NP_919224.1:n.1393-184_1393-171del