Canonical Allele Identifier: CA1239827960

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26481033_26481034delinsAG , CM000664.2:g.26481033_26481034delinsAG	GRCh38
NC_000002.11:g.26703901_26703902delinsAG , CM000664.1:g.26703901_26703902delinsAG	GRCh37
NC_000002.10:g.26557405_26557406delinsAG	NCBI36
NG_009937.1:g.82665_82666delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1580-25_1580-24delinsCT MANE Select	ENSP00000272371.2:n.1580-25_1580-24delinsCT
ENST00000272371.6:c.1580-25_1580-24delinsCT	ENSP00000272371.2:n.1580-25_1580-24delinsCT
ENST00000403946.7:c.1580-25_1580-24delinsCT	ENSP00000385255.3:n.1580-25_1580-24delinsCT
NM_001287489.1:c.1580-25_1580-24delinsCT	NP_001274418.1:n.1580-25_1580-24delinsCT
NM_194248.2:c.1580-25_1580-24delinsCT	NP_919224.1:n.1580-25_1580-24delinsCT
XM_005264644.2:c.1625-25_1625-24delinsCT	XP_005264701.1:n.1625-25_1625-24delinsCT
XM_011533185.1:c.1625-25_1625-24delinsCT	XP_011531487.1:n.1625-25_1625-24delinsCT
XM_017005338.1:c.1580-25_1580-24delinsCT	XP_016860827.1:n.1580-25_1580-24delinsCT
NM_001287489.2:c.1580-25_1580-24delinsCT	NP_001274418.1:n.1580-25_1580-24delinsCT
NM_194248.3:c.1580-25_1580-24delinsCT MANE Select	NP_919224.1:n.1580-25_1580-24delinsCT