Canonical Allele Identifier: CA531396179

Gene: OTOF

Linked Data

• dbSNP Id: rs1269353297
• gnomAD v2: 2-26705697-G-GTA
• gnomAD v3: 2-26482829-G-GTA
• gnomAD v4: 2-26482829-G-GTA
• MyVariant Identifiers: chr2:g.26705697_26705698insTA (hg19) ; chr2:g.26482829_26482830insTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482830_26482831insAT , CM000664.2:g.26482830_26482831insAT	GRCh38
NC_000002.11:g.26705698_26705699insAT , CM000664.1:g.26705698_26705699insAT	GRCh37
NC_000002.10:g.26559202_26559203insAT	NCBI36
NG_009937.1:g.80869_80870insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-238_1393-237insTA MANE Select	ENSP00000272371.2:n.1393-238_1393-237insTA
ENST00000272371.6:c.1393-238_1393-237insTA	ENSP00000272371.2:n.1393-238_1393-237insTA
ENST00000403946.7:c.1393-238_1393-237insTA	ENSP00000385255.3:n.1393-238_1393-237insTA
NM_001287489.1:c.1393-238_1393-237insTA	NP_001274418.1:n.1393-238_1393-237insTA
NM_194248.2:c.1393-238_1393-237insTA	NP_919224.1:n.1393-238_1393-237insTA
XM_005264644.2:c.1438-238_1438-237insTA	XP_005264701.1:n.1438-238_1438-237insTA
XM_011533185.1:c.1438-238_1438-237insTA	XP_011531487.1:n.1438-238_1438-237insTA
XM_017005338.1:c.1393-238_1393-237insTA	XP_016860827.1:n.1393-238_1393-237insTA
NM_001287489.2:c.1393-238_1393-237insTA	NP_001274418.1:n.1393-238_1393-237insTA
NM_194248.3:c.1393-238_1393-237insTA MANE Select	NP_919224.1:n.1393-238_1393-237insTA