Canonical Allele Identifier: CA2620017003

Gene: OTOGL

Linked Data

• gnomAD v4: 12-80358497-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358497_80358498insA , CM000674.2:g.80358497_80358498insA	GRCh38
NC_000012.11:g.80752277_80752278insA , CM000674.1:g.80752277_80752278insA	GRCh37
NC_000012.10:g.79276408_79276409insA	NCBI36
NG_033008.1:g.154045_154046insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6121+148_6121+149insA MANE Select	ENSP00000447211.2:n.6121+148_6121+149insA
ENST00000642294.1:c.61+148_61+149insA	ENSP00000493572.1:n.61+148_61+149insA
ENST00000646859.1:c.5986+148_5986+149insA	ENSP00000496036.1:n.5986+148_5986+149insA
ENST00000298820.7:c.1422+148_1422+149insA
ENST00000458043.6:c.6094+148_6094+149insA	ENSP00000400895.2:n.6094+148_6094+149insA
ENST00000546620.5:n.377+148_377+149insA
ENST00000547103.5:c.6058+148_6058+149insA	ENSP00000447211.1:n.6058+148_6058+149insA
ENST00000550182.2:c.145+148_145+149insA	ENSP00000449641.1:n.145+148_145+149insA
ENST00000551340.5:c.249+148_249+149insA
NM_173591.3:c.6094+148_6094+149insA	NP_775862.3:n.6094+148_6094+149insA
XM_005268802.2:c.6145+148_6145+149insA	XP_005268859.1:n.6145+148_6145+149insA
XM_011538191.1:c.6145+148_6145+149insA	XP_011536493.1:n.6145+148_6145+149insA
XM_011538192.1:c.5992+148_5992+149insA	XP_011536494.1:n.5992+148_5992+149insA
XM_011538193.1:c.5779+148_5779+149insA	XP_011536495.1:n.5779+148_5779+149insA
XM_005268802.3:c.6145+148_6145+149insA	XP_005268859.1:n.6145+148_6145+149insA
XM_011538192.2:c.5992+148_5992+149insA	XP_011536494.1:n.5992+148_5992+149insA
NM_001368062.1:c.5959+148_5959+149insA	NP_001354991.1:n.5959+148_5959+149insA
NM_001368062.3:c.5986+148_5986+149insA	NP_001354991.2:n.5986+148_5986+149insA
NM_001378609.3:c.6121+148_6121+149insA MANE Select	NP_001365538.2:n.6121+148_6121+149insA
NM_001378610.3:c.6121+148_6121+149insA	NP_001365539.2:n.6121+148_6121+149insA
NM_173591.7:c.6121+148_6121+149insA	NP_775862.4:n.6121+148_6121+149insA