Canonical Allele Identifier: CA2658232878

Gene: OTOF

Linked Data

• gnomAD v4: 2-26460328-C-CTGGGGCCA

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460331_26460332insGGCCATGG , CM000664.2:g.26460331_26460332insGGCCATGG	GRCh38
NC_000002.11:g.26683199_26683200insGGCCATGG , CM000664.1:g.26683199_26683200insGGCCATGG	GRCh37
NC_000002.10:g.26536703_26536704insGGCCATGG	NCBI36
NG_009937.1:g.103370_103371insTGGCCCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.5814-124_5814-123insTGGCCCCA MANE Select	ENSP00000272371.2:n.5814-124_5814-123insTGGCCCCA
ENST00000339598.8:c.3512+318_3512+319insTGGCCCCA MANE Plus Clinical	ENSP00000344521.3:n.3512+318_3512+319insTGGCCCCA
ENST00000402415.8:c.3573-124_3573-123insTGGCCCCA	ENSP00000383906.4:n.3573-124_3573-123insTGGCCCCA
ENST00000272371.6:c.5814-124_5814-123insTGGCCCCA	ENSP00000272371.2:n.5814-124_5814-123insTGGCCCCA
ENST00000338581.10:c.3513-124_3513-123insTGGCCCCA	ENSP00000345137.6:n.3513-124_3513-123insTGGCCCCA
ENST00000339598.7:c.3512+318_3512+319insTGGCCCCA	ENSP00000344521.3:n.3512+318_3512+319insTGGCCCCA
ENST00000402415.7:c.3744-124_3744-123insTGGCCCCA	ENSP00000383906.3:n.3744-124_3744-123insTGGCCCCA
ENST00000403946.7:c.5813+318_5813+319insTGGCCCCA	ENSP00000385255.3:n.5813+318_5813+319insTGGCCCCA
NM_001287489.1:c.5813+318_5813+319insTGGCCCCA	NP_001274418.1:n.5813+318_5813+319insTGGCCCCA
NM_004802.3:c.3513-124_3513-123insTGGCCCCA	NP_004793.2:n.3513-124_3513-123insTGGCCCCA
NM_194248.2:c.5814-124_5814-123insTGGCCCCA	NP_919224.1:n.5814-124_5814-123insTGGCCCCA
NM_194322.2:c.3744-124_3744-123insTGGCCCCA	NP_919303.1:n.3744-124_3744-123insTGGCCCCA
NM_194323.2:c.3512+318_3512+319insTGGCCCCA	NP_919304.1:n.3512+318_3512+319insTGGCCCCA
XM_005264644.2:c.5798+318_5798+319insTGGCCCCA	XP_005264701.1:n.5798+318_5798+319insTGGCCCCA
XM_011533185.1:c.5858+318_5858+319insTGGCCCCA	XP_011531487.1:n.5858+318_5858+319insTGGCCCCA
XM_017005338.1:c.5754-124_5754-123insTGGCCCCA	XP_016860827.1:n.5754-124_5754-123insTGGCCCCA
NM_001287489.2:c.5813+318_5813+319insTGGCCCCA	NP_001274418.1:n.5813+318_5813+319insTGGCCCCA
NM_004802.4:c.3513-124_3513-123insTGGCCCCA	NP_004793.2:n.3513-124_3513-123insTGGCCCCA
NM_194248.3:c.5814-124_5814-123insTGGCCCCA MANE Select	NP_919224.1:n.5814-124_5814-123insTGGCCCCA
NM_194322.3:c.3744-124_3744-123insTGGCCCCA	NP_919303.1:n.3744-124_3744-123insTGGCCCCA
NM_194323.3:c.3512+318_3512+319insTGGCCCCA MANE Plus Clinical	NP_919304.1:n.3512+318_3512+319insTGGCCCCA