Canonical Allele Identifier: CA916496191

Gene: OTOF

Linked Data

• dbSNP Id: rs1572438360
• gnomAD v3: 2-26482699-ATG-A
• gnomAD v4: 2-26482699-ATG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482704_26482705del , CM000664.2:g.26482704_26482705del	GRCh38
NC_000002.11:g.26705572_26705573del , CM000664.1:g.26705572_26705573del	GRCh37
NC_000002.10:g.26559076_26559077del	NCBI36
NG_009937.1:g.80998_80999del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-109_1393-108del MANE Select	ENSP00000272371.2:n.1393-109_1393-108del
ENST00000272371.6:c.1393-109_1393-108del	ENSP00000272371.2:n.1393-109_1393-108del
ENST00000403946.7:c.1393-109_1393-108del	ENSP00000385255.3:n.1393-109_1393-108del
NM_001287489.1:c.1393-109_1393-108del	NP_001274418.1:n.1393-109_1393-108del
NM_194248.2:c.1393-109_1393-108del	NP_919224.1:n.1393-109_1393-108del
XM_005264644.2:c.1438-109_1438-108del	XP_005264701.1:n.1438-109_1438-108del
XM_011533185.1:c.1438-109_1438-108del	XP_011531487.1:n.1438-109_1438-108del
XM_017005338.1:c.1393-109_1393-108del	XP_016860827.1:n.1393-109_1393-108del
NM_001287489.2:c.1393-109_1393-108del	NP_001274418.1:n.1393-109_1393-108del
NM_194248.3:c.1393-109_1393-108del MANE Select	NP_919224.1:n.1393-109_1393-108del