Canonical Allele Identifier: CA1239827414
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480499_26480501delinsGCA , CM000664.2:g.26480499_26480501delinsGCA GRCh38
NC_000002.11:g.26703367_26703369delinsGCA , CM000664.1:g.26703367_26703369delinsGCA GRCh37
NC_000002.10:g.26556871_26556873delinsGCA NCBI36
NG_009937.1:g.83198_83200delinsTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1804-190_1804-188delinsTGC MANE Select ENSP00000272371.2:n.1804-190_1804-188delinsTGC
ENST00000272371.6:c.1804-190_1804-188delinsTGC ENSP00000272371.2:n.1804-190_1804-188delinsTGC
ENST00000403946.7:c.1804-190_1804-188delinsTGC ENSP00000385255.3:n.1804-190_1804-188delinsTGC
NM_001287489.1:c.1804-190_1804-188delinsTGC NP_001274418.1:n.1804-190_1804-188delinsTGC
NM_194248.2:c.1804-190_1804-188delinsTGC NP_919224.1:n.1804-190_1804-188delinsTGC
XM_005264644.2:c.1849-190_1849-188delinsTGC XP_005264701.1:n.1849-190_1849-188delinsTGC
XM_011533185.1:c.1849-190_1849-188delinsTGC XP_011531487.1:n.1849-190_1849-188delinsTGC
XM_017005338.1:c.1804-190_1804-188delinsTGC XP_016860827.1:n.1804-190_1804-188delinsTGC
NM_001287489.2:c.1804-190_1804-188delinsTGC NP_001274418.1:n.1804-190_1804-188delinsTGC
NM_194248.3:c.1804-190_1804-188delinsTGC MANE Select NP_919224.1:n.1804-190_1804-188delinsTGC