Canonical Allele Identifier: CA2049208563

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358862T= , CM000674.2:g.80358862T=	GRCh38
NC_000012.11:g.80752642T= , CM000674.1:g.80752642T=	GRCh37
NC_000012.10:g.79276773T=	NCBI36
NG_033008.1:g.154410T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6229T= MANE Select	ENSP00000447211.2:p.Cys2077=
ENST00000642294.1:c.169T=	ENSP00000493572.1:p.Cys57=
ENST00000646859.1:c.6094T=	ENSP00000496036.1:p.Cys2032=
ENST00000298820.7:c.1527+87T=
ENST00000458043.6:c.6202T=	ENSP00000400895.2:p.Cys2068=
ENST00000546620.5:n.485T=
ENST00000547103.5:c.6166T=	ENSP00000447211.1:p.Cys2056=
ENST00000550182.2:c.253T=	ENSP00000449641.1:p.Cys85=
ENST00000551340.5:c.357T=
NM_173591.3:c.6202T=	NP_775862.3:p.Cys2068=
XM_005268802.2:c.6253T=	XP_005268859.1:p.Cys2085=
XM_011538191.1:c.6253T=	XP_011536493.1:p.Cys2085=
XM_011538192.1:c.6100T=	XP_011536494.1:p.Cys2034=
XM_011538193.1:c.5887T=	XP_011536495.1:p.Cys1963=
XM_005268802.3:c.6253T=	XP_005268859.1:p.Cys2085=
XM_011538192.2:c.6100T=	XP_011536494.1:p.Cys2034=
NM_001368062.1:c.6067T=	NP_001354991.1:p.Cys2023=
NM_001368062.3:c.6094T=	NP_001354991.2:p.Cys2032=
NM_001378609.3:c.6229T= MANE Select	NP_001365538.2:p.Cys2077=
NM_001378610.3:c.6229T=	NP_001365539.2:p.Cys2077=
NM_173591.7:c.6229T=	NP_775862.4:p.Cys2077=