Canonical Allele Identifier: CA1028610650

Gene: OTOF

Linked Data

• gnomAD v3: 2-26482779-G-GTC
• gnomAD v4: 2-26482779-G-GTC

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482780_26482781insCT , CM000664.2:g.26482780_26482781insCT	GRCh38
NC_000002.11:g.26705648_26705649insCT , CM000664.1:g.26705648_26705649insCT	GRCh37
NC_000002.10:g.26559152_26559153insCT	NCBI36
NG_009937.1:g.80919_80920insGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-188_1393-187insGA MANE Select	ENSP00000272371.2:n.1393-188_1393-187insGA
ENST00000272371.6:c.1393-188_1393-187insGA	ENSP00000272371.2:n.1393-188_1393-187insGA
ENST00000403946.7:c.1393-188_1393-187insGA	ENSP00000385255.3:n.1393-188_1393-187insGA
NM_001287489.1:c.1393-188_1393-187insGA	NP_001274418.1:n.1393-188_1393-187insGA
NM_194248.2:c.1393-188_1393-187insGA	NP_919224.1:n.1393-188_1393-187insGA
XM_005264644.2:c.1438-188_1438-187insGA	XP_005264701.1:n.1438-188_1438-187insGA
XM_011533185.1:c.1438-188_1438-187insGA	XP_011531487.1:n.1438-188_1438-187insGA
XM_017005338.1:c.1393-188_1393-187insGA	XP_016860827.1:n.1393-188_1393-187insGA
NM_001287489.2:c.1393-188_1393-187insGA	NP_001274418.1:n.1393-188_1393-187insGA
NM_194248.3:c.1393-188_1393-187insGA MANE Select	NP_919224.1:n.1393-188_1393-187insGA