Canonical Allele Identifier: CA425359988

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26700325T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26477457T>G , CM000664.2:g.26477457T>G	GRCh38
NC_000002.11:g.26700325T>G , CM000664.1:g.26700325T>G	GRCh37
NC_000002.10:g.26553829T>G	NCBI36
NG_009937.1:g.86242A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.2365A>C MANE Select	ENSP00000272371.2:p.Arg789=
ENST00000339598.8:c.124A>C MANE Plus Clinical	ENSP00000344521.3:p.Arg42=
ENST00000402415.8:c.124A>C	ENSP00000383906.4:p.Arg42=
ENST00000272371.6:c.2365A>C	ENSP00000272371.2:p.Arg789=
ENST00000338581.10:c.124A>C	ENSP00000345137.6:p.Arg42=
ENST00000339598.7:c.124A>C	ENSP00000344521.3:p.Arg42=
ENST00000402415.7:c.295A>C	ENSP00000383906.3:p.Arg99=
ENST00000403946.7:c.2365A>C	ENSP00000385255.3:p.Arg789=
NM_001287489.1:c.2365A>C	NP_001274418.1:p.Arg789=
NM_004802.3:c.124A>C	NP_004793.2:p.Arg42=
NM_194248.2:c.2365A>C	NP_919224.1:p.Arg789=
NM_194322.2:c.295A>C	NP_919303.1:p.Arg99=
NM_194323.2:c.124A>C	NP_919304.1:p.Arg42=
XM_005264644.2:c.2410A>C	XP_005264701.1:p.Arg804=
XM_011533185.1:c.2410A>C	XP_011531487.1:p.Arg804=
XM_017005338.1:c.2365A>C	XP_016860827.1:p.Arg789=
NM_001287489.2:c.2365A>C	NP_001274418.1:p.Arg789=
NM_004802.4:c.124A>C	NP_004793.2:p.Arg42=
NM_194248.3:c.2365A>C MANE Select	NP_919224.1:p.Arg789=
NM_194322.3:c.295A>C	NP_919303.1:p.Arg99=
NM_194323.3:c.124A>C MANE Plus Clinical	NP_919304.1:p.Arg42=