Canonical Allele Identifier: CA2658234867

Gene: OTOF

Linked Data

• gnomAD v4: 2-26467386-TTTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467394_26467396del , CM000664.2:g.26467394_26467396del	GRCh38
NC_000002.11:g.26690262_26690264del , CM000664.1:g.26690262_26690264del	GRCh37
NC_000002.10:g.26543766_26543768del	NCBI36
NG_009937.1:g.96310_96312del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4203_4205del MANE Select	ENSP00000272371.2:p.Lys1402del
ENST00000339598.8:c.1902_1904del MANE Plus Clinical	ENSP00000344521.3:p.Lys635del
ENST00000402415.8:c.1962_1964del	ENSP00000383906.4:p.Lys655del
ENST00000272371.6:c.4203_4205del	ENSP00000272371.2:p.Lys1402del
ENST00000338581.10:c.1902_1904del	ENSP00000345137.6:p.Lys635del
ENST00000339598.7:c.1902_1904del	ENSP00000344521.3:p.Lys635del
ENST00000402415.7:c.2133_2135del	ENSP00000383906.3:p.Lys712del
ENST00000403946.7:c.4203_4205del	ENSP00000385255.3:p.Lys1402del
NM_001287489.1:c.4203_4205del	NP_001274418.1:p.Lys1402del
NM_004802.3:c.1902_1904del	NP_004793.2:p.Lys635del
NM_194248.2:c.4203_4205del	NP_919224.1:p.Lys1402del
NM_194322.2:c.2133_2135del	NP_919303.1:p.Lys712del
NM_194323.2:c.1902_1904del	NP_919304.1:p.Lys635del
XM_005264644.2:c.4188_4190del	XP_005264701.1:p.Lys1397del
XM_011533185.1:c.4248_4250del	XP_011531487.1:p.Lys1417del
XM_017005338.1:c.4143_4145del	XP_016860827.1:p.Lys1382del
NM_001287489.2:c.4203_4205del	NP_001274418.1:p.Lys1402del
NM_004802.4:c.1902_1904del	NP_004793.2:p.Lys635del
NM_194248.3:c.4203_4205del MANE Select	NP_919224.1:p.Lys1402del
NM_194322.3:c.2133_2135del	NP_919303.1:p.Lys712del
NM_194323.3:c.1902_1904del MANE Plus Clinical	NP_919304.1:p.Lys635del