Canonical Allele Identifier: CA2049208621

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358978_80358979delinsAT , CM000674.2:g.80358978_80358979delinsAT	GRCh38
NC_000012.11:g.80752758_80752759delinsAT , CM000674.1:g.80752758_80752759delinsAT	GRCh37
NC_000012.10:g.79276889_79276890delinsAT	NCBI36
NG_033008.1:g.154526_154527delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6267+78_6267+79delinsAT MANE Select	ENSP00000447211.2:n.6267+78_6267+79delinsAT
ENST00000642294.1:c.207+78_207+79delinsAT	ENSP00000493572.1:n.207+78_207+79delinsAT
ENST00000646859.1:c.6132+78_6132+79delinsAT	ENSP00000496036.1:n.6132+78_6132+79delinsAT
ENST00000298820.7:c.1527+203_1527+204delinsAT
ENST00000458043.6:c.6240+78_6240+79delinsAT	ENSP00000400895.2:n.6240+78_6240+79delinsAT
ENST00000546620.5:n.523+78_523+79delinsAT
ENST00000547103.5:c.6204+78_6204+79delinsAT	ENSP00000447211.1:n.6204+78_6204+79delinsAT
ENST00000550182.2:c.291+78_291+79delinsAT	ENSP00000449641.1:n.291+78_291+79delinsAT
ENST00000551340.5:c.395+78_395+79delinsAT
NM_173591.3:c.6240+78_6240+79delinsAT	NP_775862.3:n.6240+78_6240+79delinsAT
XM_005268802.2:c.6291+78_6291+79delinsAT	XP_005268859.1:n.6291+78_6291+79delinsAT
XM_011538191.1:c.6291+78_6291+79delinsAT	XP_011536493.1:n.6291+78_6291+79delinsAT
XM_011538192.1:c.6138+78_6138+79delinsAT	XP_011536494.1:n.6138+78_6138+79delinsAT
XM_011538193.1:c.5925+78_5925+79delinsAT	XP_011536495.1:n.5925+78_5925+79delinsAT
XM_005268802.3:c.6291+78_6291+79delinsAT	XP_005268859.1:n.6291+78_6291+79delinsAT
XM_011538192.2:c.6138+78_6138+79delinsAT	XP_011536494.1:n.6138+78_6138+79delinsAT
NM_001368062.1:c.6105+78_6105+79delinsAT	NP_001354991.1:n.6105+78_6105+79delinsAT
NM_001368062.3:c.6132+78_6132+79delinsAT	NP_001354991.2:n.6132+78_6132+79delinsAT
NM_001378609.3:c.6267+78_6267+79delinsAT MANE Select	NP_001365538.2:n.6267+78_6267+79delinsAT
NM_001378610.3:c.6267+78_6267+79delinsAT	NP_001365539.2:n.6267+78_6267+79delinsAT
NM_173591.7:c.6267+78_6267+79delinsAT	NP_775862.4:n.6267+78_6267+79delinsAT