Canonical Allele Identifier: CA1028610307

Gene: OTOF

Linked Data

• gnomAD v3: 2-26482689-A-ATG
• gnomAD v4: 2-26482689-A-ATG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482689_26482690insTG , CM000664.2:g.26482689_26482690insTG	GRCh38
NC_000002.11:g.26705557_26705558insTG , CM000664.1:g.26705557_26705558insTG	GRCh37
NC_000002.10:g.26559061_26559062insTG	NCBI36
NG_009937.1:g.81009_81010insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-98_1393-97insCA MANE Select	ENSP00000272371.2:n.1393-98_1393-97insCA
ENST00000272371.6:c.1393-98_1393-97insCA	ENSP00000272371.2:n.1393-98_1393-97insCA
ENST00000403946.7:c.1393-98_1393-97insCA	ENSP00000385255.3:n.1393-98_1393-97insCA
NM_001287489.1:c.1393-98_1393-97insCA	NP_001274418.1:n.1393-98_1393-97insCA
NM_194248.2:c.1393-98_1393-97insCA	NP_919224.1:n.1393-98_1393-97insCA
XM_005264644.2:c.1438-98_1438-97insCA	XP_005264701.1:n.1438-98_1438-97insCA
XM_011533185.1:c.1438-98_1438-97insCA	XP_011531487.1:n.1438-98_1438-97insCA
XM_017005338.1:c.1393-98_1393-97insCA	XP_016860827.1:n.1393-98_1393-97insCA
NM_001287489.2:c.1393-98_1393-97insCA	NP_001274418.1:n.1393-98_1393-97insCA
NM_194248.3:c.1393-98_1393-97insCA MANE Select	NP_919224.1:n.1393-98_1393-97insCA