Canonical Allele Identifier: CA1239847823

Gene: OTOF

Linked Data

• dbSNP Id: rs1666613481
• gnomAD v4: 2-26519189-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26519190del , CM000664.2:g.26519190del	GRCh38
NC_000002.11:g.26742058del , CM000664.1:g.26742058del	GRCh37
NC_000002.10:g.26595562del	NCBI36
NG_009937.1:g.44509del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.228-81del MANE Select	ENSP00000272371.2:n.228-81del
ENST00000272371.6:c.228-81del	ENSP00000272371.2:n.228-81del
ENST00000403946.7:c.228-81del	ENSP00000385255.3:n.228-81del
NM_001287489.1:c.228-81del	NP_001274418.1:n.228-81del
NM_194248.2:c.228-81del	NP_919224.1:n.228-81del
XM_005264644.2:c.228-81del	XP_005264701.1:n.228-81del
XM_011533185.1:c.228-81del	XP_011531487.1:n.228-81del
XM_017005338.1:c.228-81del	XP_016860827.1:n.228-81del
NM_001287489.2:c.228-81del	NP_001274418.1:n.228-81del
NM_194248.3:c.228-81del MANE Select	NP_919224.1:n.228-81del