Canonical Allele Identifier: CA2049208545

Gene: OTOGL

Linked Data

• dbSNP Id: rs1890070165

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358818_80358821del , CM000674.2:g.80358818_80358821del	GRCh38
NC_000012.11:g.80752598_80752601del , CM000674.1:g.80752598_80752601del	GRCh37
NC_000012.10:g.79276729_79276732del	NCBI36
NG_033008.1:g.154366_154369del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6227-42_6227-39del MANE Select	ENSP00000447211.2:n.6227-42_6227-39del
ENST00000642294.1:c.167-42_167-39del	ENSP00000493572.1:n.167-42_167-39del
ENST00000646859.1:c.6092-42_6092-39del	ENSP00000496036.1:n.6092-42_6092-39del
ENST00000298820.7:c.1527+43_1527+46del
ENST00000458043.6:c.6200-42_6200-39del	ENSP00000400895.2:n.6200-42_6200-39del
ENST00000546620.5:n.483-42_483-39del
ENST00000547103.5:c.6164-42_6164-39del	ENSP00000447211.1:n.6164-42_6164-39del
ENST00000550182.2:c.251-42_251-39del	ENSP00000449641.1:n.251-42_251-39del
ENST00000551340.5:c.355-42_355-39del
NM_173591.3:c.6200-42_6200-39del	NP_775862.3:n.6200-42_6200-39del
XM_005268802.2:c.6251-42_6251-39del	XP_005268859.1:n.6251-42_6251-39del
XM_011538191.1:c.6251-42_6251-39del	XP_011536493.1:n.6251-42_6251-39del
XM_011538192.1:c.6098-42_6098-39del	XP_011536494.1:n.6098-42_6098-39del
XM_011538193.1:c.5885-42_5885-39del	XP_011536495.1:n.5885-42_5885-39del
XM_005268802.3:c.6251-42_6251-39del	XP_005268859.1:n.6251-42_6251-39del
XM_011538192.2:c.6098-42_6098-39del	XP_011536494.1:n.6098-42_6098-39del
NM_001368062.1:c.6065-42_6065-39del	NP_001354991.1:n.6065-42_6065-39del
NM_001368062.3:c.6092-42_6092-39del	NP_001354991.2:n.6092-42_6092-39del
NM_001378609.3:c.6227-42_6227-39del MANE Select	NP_001365538.2:n.6227-42_6227-39del
NM_001378610.3:c.6227-42_6227-39del	NP_001365539.2:n.6227-42_6227-39del
NM_173591.7:c.6227-42_6227-39del	NP_775862.4:n.6227-42_6227-39del