Canonical Allele Identifier: CA2049153199

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80238872_80238874delinsCTA , CM000674.2:g.80238872_80238874delinsCTA	GRCh38
NC_000012.11:g.80632652_80632654delinsCTA , CM000674.1:g.80632652_80632654delinsCTA	GRCh37
NC_000012.10:g.79156783_79156785delinsCTA	NCBI36
NG_033008.1:g.34420_34422delinsCTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.839_841delinsCTA MANE Select	ENSP00000447211.2:p.Ala280=
ENST00000643417.1:n.1499_1501delinsCTA
ENST00000646859.1:c.839_841delinsCTA	ENSP00000496036.1:p.Ala280=
ENST00000458043.6:c.812_814delinsCTA	ENSP00000400895.2:p.Ala271=
ENST00000547103.5:c.812_814delinsCTA	ENSP00000447211.1:p.Ala271=
NM_173591.3:c.812_814delinsCTA	NP_775862.3:p.Ala271=
XM_005268802.2:c.863_865delinsCTA	XP_005268859.1:p.Ala288=
XM_011538191.1:c.863_865delinsCTA	XP_011536493.1:p.Ala288=
XM_011538192.1:c.710_712delinsCTA	XP_011536494.1:p.Ala237=
XM_011538193.1:c.497_499delinsCTA	XP_011536495.1:p.Ala166=
XM_005268802.3:c.863_865delinsCTA	XP_005268859.1:p.Ala288=
XM_011538192.2:c.710_712delinsCTA	XP_011536494.1:p.Ala237=
NM_001368062.1:c.812_814delinsCTA	NP_001354991.1:p.Ala271=
NM_001368062.3:c.839_841delinsCTA	NP_001354991.2:p.Ala280=
NM_001378609.3:c.839_841delinsCTA MANE Select	NP_001365538.2:p.Ala280=
NM_001378610.3:c.839_841delinsCTA	NP_001365539.2:p.Ala280=
NM_173591.7:c.839_841delinsCTA	NP_775862.4:p.Ala280=