Canonical Allele Identifier: CA1239829575
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482868_26482872delinsCGTGT , CM000664.2:g.26482868_26482872delinsCGTGT GRCh38
NC_000002.11:g.26705736_26705740delinsCGTGT , CM000664.1:g.26705736_26705740delinsCGTGT GRCh37
NC_000002.10:g.26559240_26559244delinsCGTGT NCBI36
NG_009937.1:g.80827_80831delinsACACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1393-280_1393-276delinsACACG MANE Select ENSP00000272371.2:n.1393-280_1393-276delinsACACG
ENST00000272371.6:c.1393-280_1393-276delinsACACG ENSP00000272371.2:n.1393-280_1393-276delinsACACG
ENST00000403946.7:c.1393-280_1393-276delinsACACG ENSP00000385255.3:n.1393-280_1393-276delinsACACG
NM_001287489.1:c.1393-280_1393-276delinsACACG NP_001274418.1:n.1393-280_1393-276delinsACACG
NM_194248.2:c.1393-280_1393-276delinsACACG NP_919224.1:n.1393-280_1393-276delinsACACG
XM_005264644.2:c.1438-280_1438-276delinsACACG XP_005264701.1:n.1438-280_1438-276delinsACACG
XM_011533185.1:c.1438-280_1438-276delinsACACG XP_011531487.1:n.1438-280_1438-276delinsACACG
XM_017005338.1:c.1393-280_1393-276delinsACACG XP_016860827.1:n.1393-280_1393-276delinsACACG
NM_001287489.2:c.1393-280_1393-276delinsACACG NP_001274418.1:n.1393-280_1393-276delinsACACG
NM_194248.3:c.1393-280_1393-276delinsACACG MANE Select NP_919224.1:n.1393-280_1393-276delinsACACG