Canonical Allele Identifier: CA767288499
Gene: OTOF HGNC NCBI

Linked Data

dbSNP Id: rs1254806438

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26480786del , CM000664.2:g.26480786del GRCh38
NC_000002.11:g.26703654del , CM000664.1:g.26703654del GRCh37
NC_000002.10:g.26557158del NCBI36
NG_009937.1:g.82914del

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.1803+1del
ENST00000272371.6:c.1803+1del
ENST00000403946.7:c.1803+1del
NM_001287489.1:c.1803+1del
NM_194248.2:c.1803+1del
XM_005264644.2:c.1848+1del
XM_011533185.1:c.1848+1del
XM_017005338.1:c.1803+1del
NM_001287489.2:c.1803+1del
NM_194248.3:c.1803+1del