Canonical Allele Identifier: CA2658237336

Gene: OTOF

Linked Data

• dbSNP Id: rs754487928
• gnomAD v4: 2-26476319-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26476324del , CM000664.2:g.26476324del	GRCh38
NC_000002.11:g.26699192del , CM000664.1:g.26699192del	GRCh37
NC_000002.10:g.26552696del	NCBI36
NG_009937.1:g.87379del

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.2677-3del MANE Select	ENSP00000272371.2:n.2677-3del
ENST00000339598.8:c.436-3del MANE Plus Clinical	ENSP00000344521.3:n.436-3del
ENST00000402415.8:c.436-3del	ENSP00000383906.4:n.436-3del
ENST00000272371.6:c.2677-3del	ENSP00000272371.2:n.2677-3del
ENST00000338581.10:c.436-3del	ENSP00000345137.6:n.436-3del
ENST00000339598.7:c.436-3del	ENSP00000344521.3:n.436-3del
ENST00000402415.7:c.607-3del	ENSP00000383906.3:n.607-3del
ENST00000403946.7:c.2677-3del	ENSP00000385255.3:n.2677-3del
NM_001287489.1:c.2677-3del	NP_001274418.1:n.2677-3del
NM_004802.3:c.436-3del	NP_004793.2:n.436-3del
NM_194248.2:c.2677-3del	NP_919224.1:n.2677-3del
NM_194322.2:c.607-3del	NP_919303.1:n.607-3del
NM_194323.2:c.436-3del	NP_919304.1:n.436-3del
XM_005264644.2:c.2722-3del	XP_005264701.1:n.2722-3del
XM_011533185.1:c.2722-3del	XP_011531487.1:n.2722-3del
XM_017005338.1:c.2677-3del	XP_016860827.1:n.2677-3del
NM_001287489.2:c.2677-3del	NP_001274418.1:n.2677-3del
NM_004802.4:c.436-3del	NP_004793.2:n.436-3del
NM_194248.3:c.2677-3del MANE Select	NP_919224.1:n.2677-3del
NM_194322.3:c.607-3del	NP_919303.1:n.607-3del
NM_194323.3:c.436-3del MANE Plus Clinical	NP_919304.1:n.436-3del