Canonical Allele Identifier: CA1239824084
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26460137G= , CM000664.2:g.26460137G= GRCh38
NC_000002.11:g.26683005G= , CM000664.1:g.26683005G= GRCh37
NC_000002.10:g.26536509G= NCBI36
NG_009937.1:g.103562C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.5882C= MANE Select ENSP00000272371.2:p.Thr1961=
ENST00000339598.8:c.3512+510C= MANE Plus Clinical ENSP00000344521.3:n.3512+510C=
ENST00000402415.8:c.3641C= ENSP00000383906.4:p.Thr1214=
ENST00000272371.6:c.5882C= ENSP00000272371.2:p.Thr1961=
ENST00000338581.10:c.3581C= ENSP00000345137.6:p.Thr1194=
ENST00000339598.7:c.3512+510C= ENSP00000344521.3:n.3512+510C=
ENST00000402415.7:c.3812C= ENSP00000383906.3:p.Thr1271=
ENST00000403946.7:c.5813+510C= ENSP00000385255.3:n.5813+510C=
NM_001287489.1:c.5813+510C= NP_001274418.1:n.5813+510C=
NM_004802.3:c.3581C= NP_004793.2:p.Thr1194=
NM_194248.2:c.5882C= NP_919224.1:p.Thr1961=
NM_194322.2:c.3812C= NP_919303.1:p.Thr1271=
NM_194323.2:c.3512+510C= NP_919304.1:n.3512+510C=
XM_005264644.2:c.5798+510C= XP_005264701.1:n.5798+510C=
XM_011533185.1:c.5858+510C= XP_011531487.1:n.5858+510C=
XM_017005338.1:c.5822C= XP_016860827.1:p.Thr1941=
NM_001287489.2:c.5813+510C= NP_001274418.1:n.5813+510C=
NM_004802.4:c.3581C= NP_004793.2:p.Thr1194=
NM_194248.3:c.5882C= MANE Select NP_919224.1:p.Thr1961=
NM_194322.3:c.3812C= NP_919303.1:p.Thr1271=
NM_194323.3:c.3512+510C= MANE Plus Clinical NP_919304.1:n.3512+510C=