Canonical Allele Identifier: CA2658239253
Gene: OTOF HGNC NCBI

Linked Data

gnomAD v4: 2-26483403-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26483403G>A , CM000664.2:g.26483403G>A GRCh38
NC_000002.11:g.26706271G>A , CM000664.1:g.26706271G>A GRCh37
NC_000002.10:g.26559775G>A NCBI36
NG_009937.1:g.80296C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1392+59C>T MANE Select ENSP00000272371.2:n.1392+59C>T
ENST00000272371.6:c.1392+59C>T ENSP00000272371.2:n.1392+59C>T
ENST00000403946.7:c.1392+59C>T ENSP00000385255.3:n.1392+59C>T
NM_001287489.1:c.1392+59C>T NP_001274418.1:n.1392+59C>T
NM_194248.2:c.1392+59C>T NP_919224.1:n.1392+59C>T
XM_005264644.2:c.1437+59C>T XP_005264701.1:n.1437+59C>T
XM_011533185.1:c.1437+59C>T XP_011531487.1:n.1437+59C>T
XM_017005338.1:c.1392+59C>T XP_016860827.1:n.1392+59C>T
NM_001287489.2:c.1392+59C>T NP_001274418.1:n.1392+59C>T
NM_194248.3:c.1392+59C>T MANE Select NP_919224.1:n.1392+59C>T