Canonical Allele Identifier: CA1239830481

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26483632_26483633delinsCG , CM000664.2:g.26483632_26483633delinsCG	GRCh38
NC_000002.11:g.26706500_26706501delinsCG , CM000664.1:g.26706500_26706501delinsCG	GRCh37
NC_000002.10:g.26560004_26560005delinsCG	NCBI36
NG_009937.1:g.80066_80067delinsCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.1221_1222delinsCG MANE Select	ENSP00000272371.2:p.Pro407=
ENST00000272371.6:c.1221_1222delinsCG	ENSP00000272371.2:p.Pro407=
ENST00000403946.7:c.1221_1222delinsCG	ENSP00000385255.3:p.Pro407=
NM_001287489.1:c.1221_1222delinsCG	NP_001274418.1:p.Pro407=
NM_194248.2:c.1221_1222delinsCG	NP_919224.1:p.Pro407=
XM_005264644.2:c.1266_1267delinsCG	XP_005264701.1:p.Pro422=
XM_011533185.1:c.1266_1267delinsCG	XP_011531487.1:p.Pro422=
XM_017005338.1:c.1221_1222delinsCG	XP_016860827.1:p.Pro407=
NM_001287489.2:c.1221_1222delinsCG	NP_001274418.1:p.Pro407=
NM_194248.3:c.1221_1222delinsCG MANE Select	NP_919224.1:p.Pro407=