Canonical Allele Identifier: CA142768
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26479640G>A , CM000664.2:g.26479640G>A GRCh38
NC_000002.11:g.26702508G>A , CM000664.1:g.26702508G>A GRCh37
NC_000002.10:g.26556012G>A NCBI36
NG_009937.1:g.84059C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000272371.7:c.1926C>T MANE Select ENSP00000272371.2:p.Asn642=
ENST00000272371.6:c.1926C>T ENSP00000272371.2:p.Asn642=
ENST00000403946.7:c.1926C>T ENSP00000385255.3:p.Asn642=
NM_001287489.1:c.1926C>T NP_001274418.1:p.Asn642=
NM_194248.2:c.1926C>T NP_919224.1:p.Asn642=
XM_005264644.2:c.1971C>T XP_005264701.1:p.Asn657=
XM_011533185.1:c.1971C>T XP_011531487.1:p.Asn657=
XM_017005338.1:c.1926C>T XP_016860827.1:p.Asn642=
NM_001287489.2:c.1926C>T NP_001274418.1:p.Asn642=
NM_194248.3:c.1926C>T MANE Select NP_919224.1:p.Asn642=