Canonical Allele Identifier: CA767269916

Gene: OTOF

Linked Data

• dbSNP Id: rs1429632488
• gnomAD v4: 2-26467032-T-TG
• MyVariant Identifiers: chr2:g.26689900_26689901insG (hg19) ; chr2:g.26467032_26467033insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467037dup , CM000664.2:g.26467037dup	GRCh38
NC_000002.11:g.26689905dup , CM000664.1:g.26689905dup	GRCh37
NC_000002.10:g.26543409dup	NCBI36
NG_009937.1:g.96666dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4362+66dup MANE Select	ENSP00000272371.2:n.4362+66dup
ENST00000339598.8:c.2061+66dup MANE Plus Clinical	ENSP00000344521.3:n.2061+66dup
ENST00000402415.8:c.2121+66dup	ENSP00000383906.4:n.2121+66dup
ENST00000272371.6:c.4362+66dup	ENSP00000272371.2:n.4362+66dup
ENST00000338581.10:c.2061+66dup	ENSP00000345137.6:n.2061+66dup
ENST00000339598.7:c.2061+66dup	ENSP00000344521.3:n.2061+66dup
ENST00000402415.7:c.2292+66dup	ENSP00000383906.3:n.2292+66dup
ENST00000403946.7:c.4362+66dup	ENSP00000385255.3:n.4362+66dup
NM_001287489.1:c.4362+66dup	NP_001274418.1:n.4362+66dup
NM_004802.3:c.2061+66dup	NP_004793.2:n.2061+66dup
NM_194248.2:c.4362+66dup	NP_919224.1:n.4362+66dup
NM_194322.2:c.2292+66dup	NP_919303.1:n.2292+66dup
NM_194323.2:c.2061+66dup	NP_919304.1:n.2061+66dup
XM_005264644.2:c.4347+66dup	XP_005264701.1:n.4347+66dup
XM_011533185.1:c.4407+66dup	XP_011531487.1:n.4407+66dup
XM_017005338.1:c.4302+66dup	XP_016860827.1:n.4302+66dup
NM_001287489.2:c.4362+66dup	NP_001274418.1:n.4362+66dup
NM_004802.4:c.2061+66dup	NP_004793.2:n.2061+66dup
NM_194248.3:c.4362+66dup MANE Select	NP_919224.1:n.4362+66dup
NM_194322.3:c.2292+66dup	NP_919303.1:n.2292+66dup
NM_194323.3:c.2061+66dup MANE Plus Clinical	NP_919304.1:n.2061+66dup