Canonical Allele Identifier: CA425206658
Gene: OTOF HGNC NCBI

Linked Data

ClinVar Variation Id: 2987505
ClinVar RCV Id: RCV003849144
gnomAD v4: 2-26482527-G-A
MyVariant Identifiers: chr2:g.26705395G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482527G>A , CM000664.2:g.26482527G>A GRCh38
NC_000002.11:g.26705395G>A , CM000664.1:g.26705395G>A GRCh37
NC_000002.10:g.26558899G>A NCBI36
NG_009937.1:g.81172C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1458C>T MANE Select ENSP00000272371.2:p.Asp486=
ENST00000272371.6:c.1458C>T ENSP00000272371.2:p.Asp486=
ENST00000403946.7:c.1458C>T ENSP00000385255.3:p.Asp486=
NM_001287489.1:c.1458C>T NP_001274418.1:p.Asp486=
NM_194248.2:c.1458C>T NP_919224.1:p.Asp486=
XM_005264644.2:c.1503C>T XP_005264701.1:p.Asp501=
XM_011533185.1:c.1503C>T XP_011531487.1:p.Asp501=
XM_017005338.1:c.1458C>T XP_016860827.1:p.Asp486=
NM_001287489.2:c.1458C>T NP_001274418.1:p.Asp486=
NM_194248.3:c.1458C>T MANE Select NP_919224.1:p.Asp486=