Canonical Allele Identifier: CA1239827691
Gene: OTOF HGNC NCBI

Linked Data

dbSNP Id: rs1665517166

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480783_26480805dup , CM000664.2:g.26480783_26480805dup GRCh38
NC_000002.11:g.26703651_26703673dup , CM000664.1:g.26703651_26703673dup GRCh37
NC_000002.10:g.26557155_26557177dup NCBI36
NG_009937.1:g.82896_82918dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1786_1803+5dup
ENST00000272371.6:c.1786_1803+5dup
ENST00000403946.7:c.1786_1803+5dup
NM_001287489.1:c.1786_1803+5dup
NM_194248.2:c.1786_1803+5dup
XM_005264644.2:c.1831_1848+5dup
XM_011533185.1:c.1831_1848+5dup
XM_017005338.1:c.1786_1803+5dup
NM_001287489.2:c.1786_1803+5dup
NM_194248.3:c.1786_1803+5dup