Canonical Allele Identifier: CA2658239498

Gene: OTOF

Linked Data

• gnomAD v4: 2-26483660-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26483661dup , CM000664.2:g.26483661dup	GRCh38
NC_000002.11:g.26706529dup , CM000664.1:g.26706529dup	GRCh37
NC_000002.10:g.26560033dup	NCBI36
NG_009937.1:g.80038dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1206-13dup MANE Select	ENSP00000272371.2:n.1206-13dup
ENST00000272371.6:c.1206-13dup	ENSP00000272371.2:n.1206-13dup
ENST00000403946.7:c.1206-13dup	ENSP00000385255.3:n.1206-13dup
NM_001287489.1:c.1206-13dup	NP_001274418.1:n.1206-13dup
NM_194248.2:c.1206-13dup	NP_919224.1:n.1206-13dup
XM_005264644.2:c.1251-13dup	XP_005264701.1:n.1251-13dup
XM_011533185.1:c.1251-13dup	XP_011531487.1:n.1251-13dup
XM_017005338.1:c.1206-13dup	XP_016860827.1:n.1206-13dup
NM_001287489.2:c.1206-13dup	NP_001274418.1:n.1206-13dup
NM_194248.3:c.1206-13dup MANE Select	NP_919224.1:n.1206-13dup