Canonical Allele Identifier: CA2658238757
Gene: OTOF HGNC NCBI

Linked Data

gnomAD v4: 2-26482365-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26482365C>T , CM000664.2:g.26482365C>T GRCh38
NC_000002.11:g.26705233C>T , CM000664.1:g.26705233C>T GRCh37
NC_000002.10:g.26558737C>T NCBI36
NG_009937.1:g.81334G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.1579+41G>A MANE Select ENSP00000272371.2:n.1579+41G>A
ENST00000272371.6:c.1579+41G>A ENSP00000272371.2:n.1579+41G>A
ENST00000403946.7:c.1579+41G>A ENSP00000385255.3:n.1579+41G>A
NM_001287489.1:c.1579+41G>A NP_001274418.1:n.1579+41G>A
NM_194248.2:c.1579+41G>A NP_919224.1:n.1579+41G>A
XM_005264644.2:c.1624+41G>A XP_005264701.1:n.1624+41G>A
XM_011533185.1:c.1624+41G>A XP_011531487.1:n.1624+41G>A
XM_017005338.1:c.1579+41G>A XP_016860827.1:n.1579+41G>A
NM_001287489.2:c.1579+41G>A NP_001274418.1:n.1579+41G>A
NM_194248.3:c.1579+41G>A MANE Select NP_919224.1:n.1579+41G>A
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