Canonical Allele Identifier: CA2620016906
Gene: OTOGL HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.80358363_80358368del , CM000674.2:g.80358363_80358368del GRCh38
NC_000012.11:g.80752143_80752148del , CM000674.1:g.80752143_80752148del GRCh37
NC_000012.10:g.79276274_79276279del NCBI36
NG_033008.1:g.153911_153916del

Transcript Alleles

HGVS Amino-acid Change
ENST00000547103.7:c.6121+14_6121+19del MANE Select ENSP00000447211.2:n.6121+14_6121+19del
ENST00000642294.1:c.61+14_61+19del ENSP00000493572.1:n.61+14_61+19del
ENST00000646859.1:c.5986+14_5986+19del ENSP00000496036.1:n.5986+14_5986+19del
ENST00000298820.7:c.1422+14_1422+19del
ENST00000458043.6:c.6094+14_6094+19del ENSP00000400895.2:n.6094+14_6094+19del
ENST00000546620.5:n.377+14_377+19del
ENST00000547103.5:c.6058+14_6058+19del ENSP00000447211.1:n.6058+14_6058+19del
ENST00000550182.2:c.145+14_145+19del ENSP00000449641.1:n.145+14_145+19del
ENST00000551340.5:c.249+14_249+19del
NM_173591.3:c.6094+14_6094+19del NP_775862.3:n.6094+14_6094+19del
XM_005268802.2:c.6145+14_6145+19del XP_005268859.1:n.6145+14_6145+19del
XM_011538191.1:c.6145+14_6145+19del XP_011536493.1:n.6145+14_6145+19del
XM_011538192.1:c.5992+14_5992+19del XP_011536494.1:n.5992+14_5992+19del
XM_011538193.1:c.5779+14_5779+19del XP_011536495.1:n.5779+14_5779+19del
XM_005268802.3:c.6145+14_6145+19del XP_005268859.1:n.6145+14_6145+19del
XM_011538192.2:c.5992+14_5992+19del XP_011536494.1:n.5992+14_5992+19del
NM_001368062.1:c.5959+14_5959+19del NP_001354991.1:n.5959+14_5959+19del
NM_001368062.3:c.5986+14_5986+19del NP_001354991.2:n.5986+14_5986+19del
NM_001378609.3:c.6121+14_6121+19del MANE Select NP_001365538.2:n.6121+14_6121+19del
NM_001378610.3:c.6121+14_6121+19del NP_001365539.2:n.6121+14_6121+19del
NM_173591.7:c.6121+14_6121+19del NP_775862.4:n.6121+14_6121+19del