Canonical Allele Identifier: CA2049208574

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358885G= , CM000674.2:g.80358885G=	GRCh38
NC_000012.11:g.80752665G= , CM000674.1:g.80752665G=	GRCh37
NC_000012.10:g.79276796G=	NCBI36
NG_033008.1:g.154433G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6252G= MANE Select	ENSP00000447211.2:p.Met2084=
ENST00000642294.1:c.192G=	ENSP00000493572.1:p.Met64=
ENST00000646859.1:c.6117G=	ENSP00000496036.1:p.Met2039=
ENST00000298820.7:c.1527+110G=
ENST00000458043.6:c.6225G=	ENSP00000400895.2:p.Met2075=
ENST00000546620.5:n.508G=
ENST00000547103.5:c.6189G=	ENSP00000447211.1:p.Met2063=
ENST00000550182.2:c.276G=	ENSP00000449641.1:p.Met92=
ENST00000551340.5:c.380G=
NM_173591.3:c.6225G=	NP_775862.3:p.Met2075=
XM_005268802.2:c.6276G=	XP_005268859.1:p.Met2092=
XM_011538191.1:c.6276G=	XP_011536493.1:p.Met2092=
XM_011538192.1:c.6123G=	XP_011536494.1:p.Met2041=
XM_011538193.1:c.5910G=	XP_011536495.1:p.Met1970=
XM_005268802.3:c.6276G=	XP_005268859.1:p.Met2092=
XM_011538192.2:c.6123G=	XP_011536494.1:p.Met2041=
NM_001368062.1:c.6090G=	NP_001354991.1:p.Met2030=
NM_001368062.3:c.6117G=	NP_001354991.2:p.Met2039=
NM_001378609.3:c.6252G= MANE Select	NP_001365538.2:p.Met2084=
NM_001378610.3:c.6252G=	NP_001365539.2:p.Met2084=
NM_173591.7:c.6252G=	NP_775862.4:p.Met2084=