Canonical Allele Identifier: CA1564722
Gene: OTOF HGNC NCBI

Linked Data

dbSNP Id: rs747863126
gnomAD v2: 2-26741879-T-A
gnomAD v4: 2-26519011-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26519011T>A , CM000664.2:g.26519011T>A GRCh38
NC_000002.11:g.26741879T>A , CM000664.1:g.26741879T>A GRCh37
NC_000002.10:g.26595383T>A NCBI36
NG_009937.1:g.44688A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.326A>T MANE Select ENSP00000272371.2:p.Lys109Met
ENST00000272371.6:c.326A>T ENSP00000272371.2:p.Lys109Met
ENST00000403946.7:c.326A>T ENSP00000385255.3:p.Lys109Met
NM_001287489.1:c.326A>T NP_001274418.1:p.Lys109Met
NM_194248.2:c.326A>T NP_919224.1:p.Lys109Met
XM_005264644.2:c.326A>T XP_005264701.1:p.Lys109Met
XM_011533185.1:c.326A>T XP_011531487.1:p.Lys109Met
XM_017005338.1:c.326A>T XP_016860827.1:p.Lys109Met
NM_001287489.2:c.326A>T NP_001274418.1:p.Lys109Met
NM_194248.3:c.326A>T MANE Select NP_919224.1:p.Lys109Met