Canonical Allele Identifier: CA2576700106
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26519178_26519182dup , CM000664.2:g.26519178_26519182dup GRCh38
NC_000002.11:g.26742046_26742050dup , CM000664.1:g.26742046_26742050dup GRCh37
NC_000002.10:g.26595550_26595554dup NCBI36
NG_009937.1:g.44517_44521dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.228-73_228-69dup MANE Select ENSP00000272371.2:n.228-73_228-69dup
ENST00000272371.6:c.228-73_228-69dup ENSP00000272371.2:n.228-73_228-69dup
ENST00000403946.7:c.228-73_228-69dup ENSP00000385255.3:n.228-73_228-69dup
NM_001287489.1:c.228-73_228-69dup NP_001274418.1:n.228-73_228-69dup
NM_194248.2:c.228-73_228-69dup NP_919224.1:n.228-73_228-69dup
XM_005264644.2:c.228-73_228-69dup XP_005264701.1:n.228-73_228-69dup
XM_011533185.1:c.228-73_228-69dup XP_011531487.1:n.228-73_228-69dup
XM_017005338.1:c.228-73_228-69dup XP_016860827.1:n.228-73_228-69dup
NM_001287489.2:c.228-73_228-69dup NP_001274418.1:n.228-73_228-69dup
NM_194248.3:c.228-73_228-69dup MANE Select NP_919224.1:n.228-73_228-69dup