Canonical Allele Identifier: CA1239827909
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480979_26480980delinsAC , CM000664.2:g.26480979_26480980delinsAC GRCh38
NC_000002.11:g.26703847_26703848delinsAC , CM000664.1:g.26703847_26703848delinsAC GRCh37
NC_000002.10:g.26557351_26557352delinsAC NCBI36
NG_009937.1:g.82719_82720delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1609_1610delinsGT MANE Select ENSP00000272371.2:p.Val537=
ENST00000272371.6:c.1609_1610delinsGT ENSP00000272371.2:p.Val537=
ENST00000403946.7:c.1609_1610delinsGT ENSP00000385255.3:p.Val537=
NM_001287489.1:c.1609_1610delinsGT NP_001274418.1:p.Val537=
NM_194248.2:c.1609_1610delinsGT NP_919224.1:p.Val537=
XM_005264644.2:c.1654_1655delinsGT XP_005264701.1:p.Val552=
XM_011533185.1:c.1654_1655delinsGT XP_011531487.1:p.Val552=
XM_017005338.1:c.1609_1610delinsGT XP_016860827.1:p.Val537=
NM_001287489.2:c.1609_1610delinsGT NP_001274418.1:p.Val537=
NM_194248.3:c.1609_1610delinsGT MANE Select NP_919224.1:p.Val537=