Canonical Allele Identifier: CA1239827834
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480937_26480938delinsTC , CM000664.2:g.26480937_26480938delinsTC GRCh38
NC_000002.11:g.26703805_26703806delinsTC , CM000664.1:g.26703805_26703806delinsTC GRCh37
NC_000002.10:g.26557309_26557310delinsTC NCBI36
NG_009937.1:g.82761_82762delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1651_1652delinsGA MANE Select ENSP00000272371.2:p.Glu551=
ENST00000272371.6:c.1651_1652delinsGA ENSP00000272371.2:p.Glu551=
ENST00000403946.7:c.1651_1652delinsGA ENSP00000385255.3:p.Glu551=
NM_001287489.1:c.1651_1652delinsGA NP_001274418.1:p.Glu551=
NM_194248.2:c.1651_1652delinsGA NP_919224.1:p.Glu551=
XM_005264644.2:c.1696_1697delinsGA XP_005264701.1:p.Glu566=
XM_011533185.1:c.1696_1697delinsGA XP_011531487.1:p.Glu566=
XM_017005338.1:c.1651_1652delinsGA XP_016860827.1:p.Glu551=
NM_001287489.2:c.1651_1652delinsGA NP_001274418.1:p.Glu551=
NM_194248.3:c.1651_1652delinsGA MANE Select NP_919224.1:p.Glu551=