Canonical Allele Identifier: CA2049182448

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80302673C= , CM000674.2:g.80302673C=	GRCh38
NC_000012.11:g.80696453C= , CM000674.1:g.80696453C=	GRCh37
NC_000012.10:g.79220584C=	NCBI36
NG_033008.1:g.98221C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.3103C= MANE Select	ENSP00000447211.2:p.Gln1035=
ENST00000646859.1:c.2968C=	ENSP00000496036.1:p.Gln990=
ENST00000458043.6:c.3076C=	ENSP00000400895.2:p.Gln1026=
ENST00000547103.5:c.3076C=	ENSP00000447211.1:p.Gln1026=
NM_173591.3:c.3076C=	NP_775862.3:p.Gln1026=
XM_005268802.2:c.3127C=	XP_005268859.1:p.Gln1043=
XM_011538191.1:c.3127C=	XP_011536493.1:p.Gln1043=
XM_011538192.1:c.2974C=	XP_011536494.1:p.Gln992=
XM_011538193.1:c.2761C=	XP_011536495.1:p.Gln921=
XM_005268802.3:c.3127C=	XP_005268859.1:p.Gln1043=
XM_011538192.2:c.2974C=	XP_011536494.1:p.Gln992=
NM_001368062.1:c.2941C=	NP_001354991.1:p.Gln981=
NM_001368062.3:c.2968C=	NP_001354991.2:p.Gln990=
NM_001378609.3:c.3103C= MANE Select	NP_001365538.2:p.Gln1035=
NM_001378610.3:c.3103C=	NP_001365539.2:p.Gln1035=
NM_173591.7:c.3103C=	NP_775862.4:p.Gln1035=