Canonical Allele Identifier: CA2576699792

Gene: OTOF

Linked Data

• gnomAD v4: 2-26484709-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26484709G>T , CM000664.2:g.26484709G>T	GRCh38
NC_000002.11:g.26707577G>T , CM000664.1:g.26707577G>T	GRCh37
NC_000002.10:g.26561081G>T	NCBI36
NG_009937.1:g.78990C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1046-76C>A MANE Select	ENSP00000272371.2:n.1046-76C>A
ENST00000272371.6:c.1046-76C>A	ENSP00000272371.2:n.1046-76C>A
ENST00000403946.7:c.1046-76C>A	ENSP00000385255.3:n.1046-76C>A
NM_001287489.1:c.1046-76C>A	NP_001274418.1:n.1046-76C>A
NM_194248.2:c.1046-76C>A	NP_919224.1:n.1046-76C>A
XM_005264644.2:c.1091-76C>A	XP_005264701.1:n.1091-76C>A
XM_011533185.1:c.1091-76C>A	XP_011531487.1:n.1091-76C>A
XM_017005338.1:c.1046-76C>A	XP_016860827.1:n.1046-76C>A
NM_001287489.2:c.1046-76C>A	NP_001274418.1:n.1046-76C>A
NM_194248.3:c.1046-76C>A MANE Select	NP_919224.1:n.1046-76C>A