Canonical Allele Identifier: CA2049208575

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358886C= , CM000674.2:g.80358886C=	GRCh38
NC_000012.11:g.80752666C= , CM000674.1:g.80752666C=	GRCh37
NC_000012.10:g.79276797C=	NCBI36
NG_033008.1:g.154434C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6253C= MANE Select	ENSP00000447211.2:p.Pro2085=
ENST00000642294.1:c.193C=	ENSP00000493572.1:p.Pro65=
ENST00000646859.1:c.6118C=	ENSP00000496036.1:p.Pro2040=
ENST00000298820.7:c.1527+111C=
ENST00000458043.6:c.6226C=	ENSP00000400895.2:p.Pro2076=
ENST00000546620.5:n.509C=
ENST00000547103.5:c.6190C=	ENSP00000447211.1:p.Pro2064=
ENST00000550182.2:c.277C=	ENSP00000449641.1:p.Pro93=
ENST00000551340.5:c.381C=
NM_173591.3:c.6226C=	NP_775862.3:p.Pro2076=
XM_005268802.2:c.6277C=	XP_005268859.1:p.Pro2093=
XM_011538191.1:c.6277C=	XP_011536493.1:p.Pro2093=
XM_011538192.1:c.6124C=	XP_011536494.1:p.Pro2042=
XM_011538193.1:c.5911C=	XP_011536495.1:p.Pro1971=
XM_005268802.3:c.6277C=	XP_005268859.1:p.Pro2093=
XM_011538192.2:c.6124C=	XP_011536494.1:p.Pro2042=
NM_001368062.1:c.6091C=	NP_001354991.1:p.Pro2031=
NM_001368062.3:c.6118C=	NP_001354991.2:p.Pro2040=
NM_001378609.3:c.6253C= MANE Select	NP_001365538.2:p.Pro2085=
NM_001378610.3:c.6253C=	NP_001365539.2:p.Pro2085=
NM_173591.7:c.6253C=	NP_775862.4:p.Pro2085=