Canonical Allele Identifier: CA2658239881

Gene: OTOF

Linked Data

• gnomAD v4: 2-26484386-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26484386A>G , CM000664.2:g.26484386A>G	GRCh38
NC_000002.11:g.26707254A>G , CM000664.1:g.26707254A>G	GRCh37
NC_000002.10:g.26560758A>G	NCBI36
NG_009937.1:g.79313T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.1205+88T>C MANE Select	ENSP00000272371.2:n.1205+88T>C
ENST00000272371.6:c.1205+88T>C	ENSP00000272371.2:n.1205+88T>C
ENST00000403946.7:c.1205+88T>C	ENSP00000385255.3:n.1205+88T>C
NM_001287489.1:c.1205+88T>C	NP_001274418.1:n.1205+88T>C
NM_194248.2:c.1205+88T>C	NP_919224.1:n.1205+88T>C
XM_005264644.2:c.1250+88T>C	XP_005264701.1:n.1250+88T>C
XM_011533185.1:c.1250+88T>C	XP_011531487.1:n.1250+88T>C
XM_017005338.1:c.1205+88T>C	XP_016860827.1:n.1205+88T>C
NM_001287489.2:c.1205+88T>C	NP_001274418.1:n.1205+88T>C
NM_194248.3:c.1205+88T>C MANE Select	NP_919224.1:n.1205+88T>C