Canonical Allele Identifier: CA2049208517

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358761C= , CM000674.2:g.80358761C=	GRCh38
NC_000012.11:g.80752541C= , CM000674.1:g.80752541C=	GRCh37
NC_000012.10:g.79276672C=	NCBI36
NG_033008.1:g.154309C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6212C= MANE Select	ENSP00000447211.2:p.Pro2071=
ENST00000642294.1:c.152C=	ENSP00000493572.1:p.Pro51=
ENST00000646859.1:c.6077C=	ENSP00000496036.1:p.Pro2026=
ENST00000298820.7:c.1513C=
ENST00000458043.6:c.6185C=	ENSP00000400895.2:p.Pro2062=
ENST00000546620.5:n.468C=
ENST00000547103.5:c.6149C=	ENSP00000447211.1:p.Pro2050=
ENST00000550182.2:c.236C=	ENSP00000449641.1:p.Pro79=
ENST00000551340.5:c.340C=
NM_173591.3:c.6185C=	NP_775862.3:p.Pro2062=
XM_005268802.2:c.6236C=	XP_005268859.1:p.Pro2079=
XM_011538191.1:c.6236C=	XP_011536493.1:p.Pro2079=
XM_011538192.1:c.6083C=	XP_011536494.1:p.Pro2028=
XM_011538193.1:c.5870C=	XP_011536495.1:p.Pro1957=
XM_005268802.3:c.6236C=	XP_005268859.1:p.Pro2079=
XM_011538192.2:c.6083C=	XP_011536494.1:p.Pro2028=
NM_001368062.1:c.6050C=	NP_001354991.1:p.Pro2017=
NM_001368062.3:c.6077C=	NP_001354991.2:p.Pro2026=
NM_001378609.3:c.6212C= MANE Select	NP_001365538.2:p.Pro2071=
NM_001378610.3:c.6212C=	NP_001365539.2:p.Pro2071=
NM_173591.7:c.6212C=	NP_775862.4:p.Pro2071=