Canonical Allele Identifier: CA1239827090
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480146_26480147delinsGC , CM000664.2:g.26480146_26480147delinsGC GRCh38
NC_000002.11:g.26703014_26703015delinsGC , CM000664.1:g.26703014_26703015delinsGC GRCh37
NC_000002.10:g.26556518_26556519delinsGC NCBI36
NG_009937.1:g.83552_83553delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.1912+56_1912+57delinsGC MANE Select ENSP00000272371.2:n.1912+56_1912+57delinsGC
ENST00000272371.6:c.1912+56_1912+57delinsGC ENSP00000272371.2:n.1912+56_1912+57delinsGC
ENST00000403946.7:c.1912+56_1912+57delinsGC ENSP00000385255.3:n.1912+56_1912+57delinsGC
NM_001287489.1:c.1912+56_1912+57delinsGC NP_001274418.1:n.1912+56_1912+57delinsGC
NM_194248.2:c.1912+56_1912+57delinsGC NP_919224.1:n.1912+56_1912+57delinsGC
XM_005264644.2:c.1957+56_1957+57delinsGC XP_005264701.1:n.1957+56_1957+57delinsGC
XM_011533185.1:c.1957+56_1957+57delinsGC XP_011531487.1:n.1957+56_1957+57delinsGC
XM_017005338.1:c.1912+56_1912+57delinsGC XP_016860827.1:n.1912+56_1912+57delinsGC
NM_001287489.2:c.1912+56_1912+57delinsGC NP_001274418.1:n.1912+56_1912+57delinsGC
NM_194248.3:c.1912+56_1912+57delinsGC MANE Select NP_919224.1:n.1912+56_1912+57delinsGC