Canonical Allele Identifier: CA767290319

Gene: OTOF

Linked Data

• dbSNP Id: rs1336781623
• gnomAD v3: 2-26482805-G-GCA
• gnomAD v4: 2-26482805-G-GCA
• MyVariant Identifiers: chr2:g.26705673_26705674insCA (hg19) ; chr2:g.26482805_26482806insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482805_26482806insCA , CM000664.2:g.26482805_26482806insCA	GRCh38
NC_000002.11:g.26705673_26705674insCA , CM000664.1:g.26705673_26705674insCA	GRCh37
NC_000002.10:g.26559177_26559178insCA	NCBI36
NG_009937.1:g.80893_80894insTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1393-214_1393-213insTG MANE Select	ENSP00000272371.2:n.1393-214_1393-213insTG
ENST00000272371.6:c.1393-214_1393-213insTG	ENSP00000272371.2:n.1393-214_1393-213insTG
ENST00000403946.7:c.1393-214_1393-213insTG	ENSP00000385255.3:n.1393-214_1393-213insTG
NM_001287489.1:c.1393-214_1393-213insTG	NP_001274418.1:n.1393-214_1393-213insTG
NM_194248.2:c.1393-214_1393-213insTG	NP_919224.1:n.1393-214_1393-213insTG
XM_005264644.2:c.1438-214_1438-213insTG	XP_005264701.1:n.1438-214_1438-213insTG
XM_011533185.1:c.1438-214_1438-213insTG	XP_011531487.1:n.1438-214_1438-213insTG
XM_017005338.1:c.1393-214_1393-213insTG	XP_016860827.1:n.1393-214_1393-213insTG
NM_001287489.2:c.1393-214_1393-213insTG	NP_001274418.1:n.1393-214_1393-213insTG
NM_194248.3:c.1393-214_1393-213insTG MANE Select	NP_919224.1:n.1393-214_1393-213insTG