Canonical Allele Identifier: CA1239829393

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482748_26482749delinsTG , CM000664.2:g.26482748_26482749delinsTG	GRCh38
NC_000002.11:g.26705616_26705617delinsTG , CM000664.1:g.26705616_26705617delinsTG	GRCh37
NC_000002.10:g.26559120_26559121delinsTG	NCBI36
NG_009937.1:g.80950_80951delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-157_1393-156delinsCA MANE Select	ENSP00000272371.2:n.1393-157_1393-156delinsCA
ENST00000272371.6:c.1393-157_1393-156delinsCA	ENSP00000272371.2:n.1393-157_1393-156delinsCA
ENST00000403946.7:c.1393-157_1393-156delinsCA	ENSP00000385255.3:n.1393-157_1393-156delinsCA
NM_001287489.1:c.1393-157_1393-156delinsCA	NP_001274418.1:n.1393-157_1393-156delinsCA
NM_194248.2:c.1393-157_1393-156delinsCA	NP_919224.1:n.1393-157_1393-156delinsCA
XM_005264644.2:c.1438-157_1438-156delinsCA	XP_005264701.1:n.1438-157_1438-156delinsCA
XM_011533185.1:c.1438-157_1438-156delinsCA	XP_011531487.1:n.1438-157_1438-156delinsCA
XM_017005338.1:c.1393-157_1393-156delinsCA	XP_016860827.1:n.1393-157_1393-156delinsCA
NM_001287489.2:c.1393-157_1393-156delinsCA	NP_001274418.1:n.1393-157_1393-156delinsCA
NM_194248.3:c.1393-157_1393-156delinsCA MANE Select	NP_919224.1:n.1393-157_1393-156delinsCA