Canonical Allele Identifier: CA1239822165
Gene: OTOF HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26458094C= , CM000664.2:g.26458094C= GRCh38
NC_000002.11:g.26680962C= , CM000664.1:g.26680962C= GRCh37
NC_000002.10:g.26534466C= NCBI36
NG_009937.1:g.105605G=
NG_042824.1:g.61183C=

Transcript Alleles

HGVS Amino-acid change
ENST00000272371.7:c.*144G= MANE Select ENSP00000272371.2:n.*144G=
ENST00000339598.8:c.3639G= MANE Plus Clinical ENSP00000344521.3:p.Gly1213=
ENST00000402415.8:c.*144G= ENSP00000383906.4:n.*144G=
ENST00000272371.6:c.*144G= ENSP00000272371.2:n.*144G=
ENST00000338581.10:c.*144G= ENSP00000345137.6:n.*144G=
ENST00000339598.7:c.3639G= ENSP00000344521.3:p.Gly1213=
ENST00000402415.7:c.*144G= ENSP00000383906.3:n.*144G=
ENST00000403946.7:c.5940G= ENSP00000385255.3:p.Gly1980=
NM_001287489.1:c.5940G= NP_001274418.1:p.Gly1980=
NM_004802.3:c.*144G= NP_004793.2:n.*144G=
NM_194248.2:c.*144G= NP_919224.1:n.*144G=
NM_194322.2:c.*144G= NP_919303.1:n.*144G=
NM_194323.2:c.3639G= NP_919304.1:p.Gly1213=
XM_005264644.2:c.5925G= XP_005264701.1:p.Gly1975=
XM_011533185.1:c.5985G= XP_011531487.1:p.Gly1995=
NM_001287489.2:c.5940G= NP_001274418.1:p.Gly1980=
NM_004802.4:c.*144G= NP_004793.2:n.*144G=
NM_194248.3:c.*144G= MANE Select NP_919224.1:n.*144G=
NM_194322.3:c.*144G= NP_919303.1:n.*144G=
NM_194323.3:c.3639G= MANE Plus Clinical NP_919304.1:p.Gly1213=