Canonical Allele Identifier: CA2572418482
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26479879_26479880insGGG , CM000664.2:g.26479879_26479880insGGG GRCh38
NC_000002.11:g.26702747_26702748insGGG , CM000664.1:g.26702747_26702748insGGG GRCh37
NC_000002.10:g.26556251_26556252insGGG NCBI36
NG_009937.1:g.83821_83822insCCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1913-225_1913-224insCCC MANE Select ENSP00000272371.2:n.1913-225_1913-224insCCC
ENST00000272371.6:c.1913-225_1913-224insCCC ENSP00000272371.2:n.1913-225_1913-224insCCC
ENST00000403946.7:c.1913-225_1913-224insCCC ENSP00000385255.3:n.1913-225_1913-224insCCC
NM_001287489.1:c.1913-225_1913-224insCCC NP_001274418.1:n.1913-225_1913-224insCCC
NM_194248.2:c.1913-225_1913-224insCCC NP_919224.1:n.1913-225_1913-224insCCC
XM_005264644.2:c.1958-225_1958-224insCCC XP_005264701.1:n.1958-225_1958-224insCCC
XM_011533185.1:c.1958-225_1958-224insCCC XP_011531487.1:n.1958-225_1958-224insCCC
XM_017005338.1:c.1913-225_1913-224insCCC XP_016860827.1:n.1913-225_1913-224insCCC
NM_001287489.2:c.1913-225_1913-224insCCC NP_001274418.1:n.1913-225_1913-224insCCC
NM_194248.3:c.1913-225_1913-224insCCC MANE Select NP_919224.1:n.1913-225_1913-224insCCC