Canonical Allele Identifier: CA692353625

Gene: OTOGL

Linked Data

• dbSNP Id: rs1338015293
• gnomAD v3: 12-80358432-C-CA
• gnomAD v4: 12-80358432-C-CA
• MyVariant Identifiers: chr12:g.80752212_80752213insA (hg19) ; chr12:g.80358432_80358433insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.80358433dup , CM000674.2:g.80358433dup	GRCh38
NC_000012.11:g.80752213dup , CM000674.1:g.80752213dup	GRCh37
NC_000012.10:g.79276344dup	NCBI36
NG_033008.1:g.153981dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000547103.7:c.6121+84dup MANE Select	ENSP00000447211.2:n.6121+84dup
ENST00000642294.1:c.61+84dup	ENSP00000493572.1:n.61+84dup
ENST00000646859.1:c.5986+84dup	ENSP00000496036.1:n.5986+84dup
ENST00000298820.7:c.1422+84dup
ENST00000458043.6:c.6094+84dup	ENSP00000400895.2:n.6094+84dup
ENST00000546620.5:n.377+84dup
ENST00000547103.5:c.6058+84dup	ENSP00000447211.1:n.6058+84dup
ENST00000550182.2:c.145+84dup	ENSP00000449641.1:n.145+84dup
ENST00000551340.5:c.249+84dup
NM_173591.3:c.6094+84dup	NP_775862.3:n.6094+84dup
XM_005268802.2:c.6145+84dup	XP_005268859.1:n.6145+84dup
XM_011538191.1:c.6145+84dup	XP_011536493.1:n.6145+84dup
XM_011538192.1:c.5992+84dup	XP_011536494.1:n.5992+84dup
XM_011538193.1:c.5779+84dup	XP_011536495.1:n.5779+84dup
XM_005268802.3:c.6145+84dup	XP_005268859.1:n.6145+84dup
XM_011538192.2:c.5992+84dup	XP_011536494.1:n.5992+84dup
NM_001368062.1:c.5959+84dup	NP_001354991.1:n.5959+84dup
NM_001368062.3:c.5986+84dup	NP_001354991.2:n.5986+84dup
NM_001378609.3:c.6121+84dup MANE Select	NP_001365538.2:n.6121+84dup
NM_001378610.3:c.6121+84dup	NP_001365539.2:n.6121+84dup
NM_173591.7:c.6121+84dup	NP_775862.4:n.6121+84dup