Canonical Allele Identifier: CA1239829385

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482744_26482748delinsCGTGT , CM000664.2:g.26482744_26482748delinsCGTGT	GRCh38
NC_000002.11:g.26705612_26705616delinsCGTGT , CM000664.1:g.26705612_26705616delinsCGTGT	GRCh37
NC_000002.10:g.26559116_26559120delinsCGTGT	NCBI36
NG_009937.1:g.80951_80955delinsACACG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-156_1393-152delinsACACG MANE Select	ENSP00000272371.2:n.1393-156_1393-152delinsACACG
ENST00000272371.6:c.1393-156_1393-152delinsACACG	ENSP00000272371.2:n.1393-156_1393-152delinsACACG
ENST00000403946.7:c.1393-156_1393-152delinsACACG	ENSP00000385255.3:n.1393-156_1393-152delinsACACG
NM_001287489.1:c.1393-156_1393-152delinsACACG	NP_001274418.1:n.1393-156_1393-152delinsACACG
NM_194248.2:c.1393-156_1393-152delinsACACG	NP_919224.1:n.1393-156_1393-152delinsACACG
XM_005264644.2:c.1438-156_1438-152delinsACACG	XP_005264701.1:n.1438-156_1438-152delinsACACG
XM_011533185.1:c.1438-156_1438-152delinsACACG	XP_011531487.1:n.1438-156_1438-152delinsACACG
XM_017005338.1:c.1393-156_1393-152delinsACACG	XP_016860827.1:n.1393-156_1393-152delinsACACG
NM_001287489.2:c.1393-156_1393-152delinsACACG	NP_001274418.1:n.1393-156_1393-152delinsACACG
NM_194248.3:c.1393-156_1393-152delinsACACG MANE Select	NP_919224.1:n.1393-156_1393-152delinsACACG