Canonical Allele Identifier: CA2575235833

Gene: OTOGL

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358634_80358635del , CM000674.2:g.80358634_80358635del	GRCh38
NC_000012.11:g.80752414_80752415del , CM000674.1:g.80752414_80752415del	GRCh37
NC_000012.10:g.79276545_79276546del	NCBI36
NG_033008.1:g.154182_154183del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6122-37_6122-36del MANE Select	ENSP00000447211.2:n.6122-37_6122-36del
ENST00000642294.1:c.62-37_62-36del	ENSP00000493572.1:n.62-37_62-36del
ENST00000646859.1:c.5987-37_5987-36del	ENSP00000496036.1:n.5987-37_5987-36del
ENST00000298820.7:c.1423-37_1423-36del
ENST00000458043.6:c.6095-37_6095-36del	ENSP00000400895.2:n.6095-37_6095-36del
ENST00000546620.5:n.378-37_378-36del
ENST00000547103.5:c.6059-37_6059-36del	ENSP00000447211.1:n.6059-37_6059-36del
ENST00000550182.2:c.146-37_146-36del	ENSP00000449641.1:n.146-37_146-36del
ENST00000551340.5:c.250-37_250-36del
NM_173591.3:c.6095-37_6095-36del	NP_775862.3:n.6095-37_6095-36del
XM_005268802.2:c.6146-37_6146-36del	XP_005268859.1:n.6146-37_6146-36del
XM_011538191.1:c.6146-37_6146-36del	XP_011536493.1:n.6146-37_6146-36del
XM_011538192.1:c.5993-37_5993-36del	XP_011536494.1:n.5993-37_5993-36del
XM_011538193.1:c.5780-37_5780-36del	XP_011536495.1:n.5780-37_5780-36del
XM_005268802.3:c.6146-37_6146-36del	XP_005268859.1:n.6146-37_6146-36del
XM_011538192.2:c.5993-37_5993-36del	XP_011536494.1:n.5993-37_5993-36del
NM_001368062.1:c.5960-37_5960-36del	NP_001354991.1:n.5960-37_5960-36del
NM_001368062.3:c.5987-37_5987-36del	NP_001354991.2:n.5987-37_5987-36del
NM_001378609.3:c.6122-37_6122-36del MANE Select	NP_001365538.2:n.6122-37_6122-36del
NM_001378610.3:c.6122-37_6122-36del	NP_001365539.2:n.6122-37_6122-36del
NM_173591.7:c.6122-37_6122-36del	NP_775862.4:n.6122-37_6122-36del