Canonical Allele Identifier: CA531396128

Gene: OTOF

Linked Data

• gnomAD v2: 2-26705627-GCA-G
• gnomAD v3: 2-26482759-GCA-G
• gnomAD v4: 2-26482759-GCA-G
• MyVariant Identifiers: chr2:g.26705628_26705629del (hg19) ; chr2:g.26482760_26482761del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482760_26482761del , CM000664.2:g.26482760_26482761del	GRCh38
NC_000002.11:g.26705628_26705629del , CM000664.1:g.26705628_26705629del	GRCh37
NC_000002.10:g.26559132_26559133del	NCBI36
NG_009937.1:g.80938_80939del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-169_1393-168del MANE Select	ENSP00000272371.2:n.1393-169_1393-168del
ENST00000272371.6:c.1393-169_1393-168del	ENSP00000272371.2:n.1393-169_1393-168del
ENST00000403946.7:c.1393-169_1393-168del	ENSP00000385255.3:n.1393-169_1393-168del
NM_001287489.1:c.1393-169_1393-168del	NP_001274418.1:n.1393-169_1393-168del
NM_194248.2:c.1393-169_1393-168del	NP_919224.1:n.1393-169_1393-168del
XM_005264644.2:c.1438-169_1438-168del	XP_005264701.1:n.1438-169_1438-168del
XM_011533185.1:c.1438-169_1438-168del	XP_011531487.1:n.1438-169_1438-168del
XM_017005338.1:c.1393-169_1393-168del	XP_016860827.1:n.1393-169_1393-168del
NM_001287489.2:c.1393-169_1393-168del	NP_001274418.1:n.1393-169_1393-168del
NM_194248.3:c.1393-169_1393-168del MANE Select	NP_919224.1:n.1393-169_1393-168del