Canonical Allele Identifier: CA2049208511

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358746C= , CM000674.2:g.80358746C=	GRCh38
NC_000012.11:g.80752526C= , CM000674.1:g.80752526C=	GRCh37
NC_000012.10:g.79276657C=	NCBI36
NG_033008.1:g.154294C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6197C= MANE Select	ENSP00000447211.2:p.Ser2066=
ENST00000642294.1:c.137C=	ENSP00000493572.1:p.Ser46=
ENST00000646859.1:c.6062C=	ENSP00000496036.1:p.Ser2021=
ENST00000298820.7:c.1498C=
ENST00000458043.6:c.6170C=	ENSP00000400895.2:p.Ser2057=
ENST00000546620.5:n.453C=
ENST00000547103.5:c.6134C=	ENSP00000447211.1:p.Ser2045=
ENST00000550182.2:c.221C=	ENSP00000449641.1:p.Ser74=
ENST00000551340.5:c.325C=
NM_173591.3:c.6170C=	NP_775862.3:p.Ser2057=
XM_005268802.2:c.6221C=	XP_005268859.1:p.Ser2074=
XM_011538191.1:c.6221C=	XP_011536493.1:p.Ser2074=
XM_011538192.1:c.6068C=	XP_011536494.1:p.Ser2023=
XM_011538193.1:c.5855C=	XP_011536495.1:p.Ser1952=
XM_005268802.3:c.6221C=	XP_005268859.1:p.Ser2074=
XM_011538192.2:c.6068C=	XP_011536494.1:p.Ser2023=
NM_001368062.1:c.6035C=	NP_001354991.1:p.Ser2012=
NM_001368062.3:c.6062C=	NP_001354991.2:p.Ser2021=
NM_001378609.3:c.6197C= MANE Select	NP_001365538.2:p.Ser2066=
NM_001378610.3:c.6197C=	NP_001365539.2:p.Ser2066=
NM_173591.7:c.6197C=	NP_775862.4:p.Ser2066=