Canonical Allele Identifier: CA2658238592
Gene: OTOF HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26481071_26481072insACCCCCAAAA , CM000664.2:g.26481071_26481072insACCCCCAAAA GRCh38
NC_000002.11:g.26703939_26703940insACCCCCAAAA , CM000664.1:g.26703939_26703940insACCCCCAAAA GRCh37
NC_000002.10:g.26557443_26557444insACCCCCAAAA NCBI36
NG_009937.1:g.82627_82628insTTTTGGGGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1580-63_1580-62insTTTTGGGGGT MANE Select ENSP00000272371.2:n.1580-63_1580-62insTTTTGGGGGT
ENST00000272371.6:c.1580-63_1580-62insTTTTGGGGGT ENSP00000272371.2:n.1580-63_1580-62insTTTTGGGGGT
ENST00000403946.7:c.1580-63_1580-62insTTTTGGGGGT ENSP00000385255.3:n.1580-63_1580-62insTTTTGGGGGT
NM_001287489.1:c.1580-63_1580-62insTTTTGGGGGT NP_001274418.1:n.1580-63_1580-62insTTTTGGGGGT
NM_194248.2:c.1580-63_1580-62insTTTTGGGGGT NP_919224.1:n.1580-63_1580-62insTTTTGGGGGT
XM_005264644.2:c.1625-63_1625-62insTTTTGGGGGT XP_005264701.1:n.1625-63_1625-62insTTTTGGGGGT
XM_011533185.1:c.1625-63_1625-62insTTTTGGGGGT XP_011531487.1:n.1625-63_1625-62insTTTTGGGGGT
XM_017005338.1:c.1580-63_1580-62insTTTTGGGGGT XP_016860827.1:n.1580-63_1580-62insTTTTGGGGGT
NM_001287489.2:c.1580-63_1580-62insTTTTGGGGGT NP_001274418.1:n.1580-63_1580-62insTTTTGGGGGT
NM_194248.3:c.1580-63_1580-62insTTTTGGGGGT MANE Select NP_919224.1:n.1580-63_1580-62insTTTTGGGGGT