Canonical Allele Identifier: CA2049199534

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80339228C= , CM000674.2:g.80339228C=	GRCh38
NC_000012.11:g.80733008C= , CM000674.1:g.80733008C=	GRCh37
NC_000012.10:g.79257139C=	NCBI36
NG_033008.1:g.134776C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.5014C= MANE Select	ENSP00000447211.2:p.Arg1672=
ENST00000646859.1:c.4879C=	ENSP00000496036.1:p.Arg1627=
ENST00000298820.7:c.315C=
ENST00000458043.6:c.4987C=	ENSP00000400895.2:p.Arg1663=
ENST00000547103.5:c.4951C=	ENSP00000447211.1:p.Arg1651=
NM_173591.3:c.4987C=	NP_775862.3:p.Arg1663=
XM_005268802.2:c.5038C=	XP_005268859.1:p.Arg1680=
XM_011538191.1:c.5038C=	XP_011536493.1:p.Arg1680=
XM_011538192.1:c.4885C=	XP_011536494.1:p.Arg1629=
XM_011538193.1:c.4672C=	XP_011536495.1:p.Arg1558=
XM_005268802.3:c.5038C=	XP_005268859.1:p.Arg1680=
XM_011538192.2:c.4885C=	XP_011536494.1:p.Arg1629=
NM_001368062.1:c.4852C=	NP_001354991.1:p.Arg1618=
NM_001368062.3:c.4879C=	NP_001354991.2:p.Arg1627=
NM_001378609.3:c.5014C= MANE Select	NP_001365538.2:p.Arg1672=
NM_001378610.3:c.5014C=	NP_001365539.2:p.Arg1672=
NM_173591.7:c.5014C=	NP_775862.4:p.Arg1672=