Canonical Allele Identifier: CA2049208491

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358694A= , CM000674.2:g.80358694A=	GRCh38
NC_000012.11:g.80752474A= , CM000674.1:g.80752474A=	GRCh37
NC_000012.10:g.79276605A=	NCBI36
NG_033008.1:g.154242A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6145A= MANE Select	ENSP00000447211.2:p.Met2049=
ENST00000642294.1:c.85A=	ENSP00000493572.1:p.Met29=
ENST00000646859.1:c.6010A=	ENSP00000496036.1:p.Met2004=
ENST00000298820.7:c.1446A=
ENST00000458043.6:c.6118A=	ENSP00000400895.2:p.Met2040=
ENST00000546620.5:n.401A=
ENST00000547103.5:c.6082A=	ENSP00000447211.1:p.Met2028=
ENST00000550182.2:c.169A=	ENSP00000449641.1:p.Met57=
ENST00000551340.5:c.273A=
NM_173591.3:c.6118A=	NP_775862.3:p.Met2040=
XM_005268802.2:c.6169A=	XP_005268859.1:p.Met2057=
XM_011538191.1:c.6169A=	XP_011536493.1:p.Met2057=
XM_011538192.1:c.6016A=	XP_011536494.1:p.Met2006=
XM_011538193.1:c.5803A=	XP_011536495.1:p.Met1935=
XM_005268802.3:c.6169A=	XP_005268859.1:p.Met2057=
XM_011538192.2:c.6016A=	XP_011536494.1:p.Met2006=
NM_001368062.1:c.5983A=	NP_001354991.1:p.Met1995=
NM_001368062.3:c.6010A=	NP_001354991.2:p.Met2004=
NM_001378609.3:c.6145A= MANE Select	NP_001365538.2:p.Met2049=
NM_001378610.3:c.6145A=	NP_001365539.2:p.Met2049=
NM_173591.7:c.6145A=	NP_775862.4:p.Met2049=