Canonical Allele Identifier: CA2658238456

Gene: OTOF

Linked Data

• gnomAD v4: 2-26481014-G-GTTC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26481014_26481015insTTC , CM000664.2:g.26481014_26481015insTTC	GRCh38
NC_000002.11:g.26703882_26703883insTTC , CM000664.1:g.26703882_26703883insTTC	GRCh37
NC_000002.10:g.26557386_26557387insTTC	NCBI36
NG_009937.1:g.82684_82685insGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1580-6_1580-5insGAA MANE Select	ENSP00000272371.2:n.1580-6_1580-5insGAA
ENST00000272371.6:c.1580-6_1580-5insGAA	ENSP00000272371.2:n.1580-6_1580-5insGAA
ENST00000403946.7:c.1580-6_1580-5insGAA	ENSP00000385255.3:n.1580-6_1580-5insGAA
NM_001287489.1:c.1580-6_1580-5insGAA	NP_001274418.1:n.1580-6_1580-5insGAA
NM_194248.2:c.1580-6_1580-5insGAA	NP_919224.1:n.1580-6_1580-5insGAA
XM_005264644.2:c.1625-6_1625-5insGAA	XP_005264701.1:n.1625-6_1625-5insGAA
XM_011533185.1:c.1625-6_1625-5insGAA	XP_011531487.1:n.1625-6_1625-5insGAA
XM_017005338.1:c.1580-6_1580-5insGAA	XP_016860827.1:n.1580-6_1580-5insGAA
NM_001287489.2:c.1580-6_1580-5insGAA	NP_001274418.1:n.1580-6_1580-5insGAA
NM_194248.3:c.1580-6_1580-5insGAA MANE Select	NP_919224.1:n.1580-6_1580-5insGAA