Canonical Allele Identifier: CA2658238021

Gene: OTOF

Linked Data

• gnomAD v4: 2-26480398-CGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26480400_26480401del , CM000664.2:g.26480400_26480401del	GRCh38
NC_000002.11:g.26703268_26703269del , CM000664.1:g.26703268_26703269del	GRCh37
NC_000002.10:g.26556772_26556773del	NCBI36
NG_009937.1:g.83299_83300del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1804-89_1804-88del MANE Select	ENSP00000272371.2:n.1804-89_1804-88del
ENST00000272371.6:c.1804-89_1804-88del	ENSP00000272371.2:n.1804-89_1804-88del
ENST00000403946.7:c.1804-89_1804-88del	ENSP00000385255.3:n.1804-89_1804-88del
NM_001287489.1:c.1804-89_1804-88del	NP_001274418.1:n.1804-89_1804-88del
NM_194248.2:c.1804-89_1804-88del	NP_919224.1:n.1804-89_1804-88del
XM_005264644.2:c.1849-89_1849-88del	XP_005264701.1:n.1849-89_1849-88del
XM_011533185.1:c.1849-89_1849-88del	XP_011531487.1:n.1849-89_1849-88del
XM_017005338.1:c.1804-89_1804-88del	XP_016860827.1:n.1804-89_1804-88del
NM_001287489.2:c.1804-89_1804-88del	NP_001274418.1:n.1804-89_1804-88del
NM_194248.3:c.1804-89_1804-88del MANE Select	NP_919224.1:n.1804-89_1804-88del