Canonical Allele Identifier: CA346139789
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26519095A>T , CM000664.2:g.26519095A>T GRCh38
NC_000002.11:g.26741963A>T , CM000664.1:g.26741963A>T GRCh37
NC_000002.10:g.26595467A>T NCBI36
NG_009937.1:g.44604T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.242T>A MANE Select ENSP00000272371.2:p.Phe81Tyr
ENST00000272371.6:c.242T>A ENSP00000272371.2:p.Phe81Tyr
ENST00000403946.7:c.242T>A ENSP00000385255.3:p.Phe81Tyr
NM_001287489.1:c.242T>A NP_001274418.1:p.Phe81Tyr
NM_194248.2:c.242T>A NP_919224.1:p.Phe81Tyr
XM_005264644.2:c.242T>A XP_005264701.1:p.Phe81Tyr
XM_011533185.1:c.242T>A XP_011531487.1:p.Phe81Tyr
XM_017005338.1:c.242T>A XP_016860827.1:p.Phe81Tyr
NM_001287489.2:c.242T>A NP_001274418.1:p.Phe81Tyr
NM_194248.3:c.242T>A MANE Select NP_919224.1:p.Phe81Tyr