Canonical Allele Identifier: CA2658238594

Gene: OTOF

Linked Data

• gnomAD v4: 2-26481072-G-GAGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26481072_26481073insAGGCC , CM000664.2:g.26481072_26481073insAGGCC	GRCh38
NC_000002.11:g.26703940_26703941insAGGCC , CM000664.1:g.26703940_26703941insAGGCC	GRCh37
NC_000002.10:g.26557444_26557445insAGGCC	NCBI36
NG_009937.1:g.82626_82627insGGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1580-64_1580-63insGGCCT MANE Select	ENSP00000272371.2:n.1580-64_1580-63insGGCCT
ENST00000272371.6:c.1580-64_1580-63insGGCCT	ENSP00000272371.2:n.1580-64_1580-63insGGCCT
ENST00000403946.7:c.1580-64_1580-63insGGCCT	ENSP00000385255.3:n.1580-64_1580-63insGGCCT
NM_001287489.1:c.1580-64_1580-63insGGCCT	NP_001274418.1:n.1580-64_1580-63insGGCCT
NM_194248.2:c.1580-64_1580-63insGGCCT	NP_919224.1:n.1580-64_1580-63insGGCCT
XM_005264644.2:c.1625-64_1625-63insGGCCT	XP_005264701.1:n.1625-64_1625-63insGGCCT
XM_011533185.1:c.1625-64_1625-63insGGCCT	XP_011531487.1:n.1625-64_1625-63insGGCCT
XM_017005338.1:c.1580-64_1580-63insGGCCT	XP_016860827.1:n.1580-64_1580-63insGGCCT
NM_001287489.2:c.1580-64_1580-63insGGCCT	NP_001274418.1:n.1580-64_1580-63insGGCCT
NM_194248.3:c.1580-64_1580-63insGGCCT MANE Select	NP_919224.1:n.1580-64_1580-63insGGCCT