Canonical Allele Identifier: CA425201625

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26693470G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26470602G>C , CM000664.2:g.26470602G>C	GRCh38
NC_000002.11:g.26693470G>C , CM000664.1:g.26693470G>C	GRCh37
NC_000002.10:g.26546974G>C	NCBI36
NG_009937.1:g.93097C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.4014C>G MANE Select	ENSP00000272371.2:p.Thr1338=
ENST00000339598.8:c.1713C>G MANE Plus Clinical	ENSP00000344521.3:p.Thr571=
ENST00000402415.8:c.1773C>G	ENSP00000383906.4:p.Thr591=
ENST00000272371.6:c.4014C>G	ENSP00000272371.2:p.Thr1338=
ENST00000338581.10:c.1713C>G	ENSP00000345137.6:p.Thr571=
ENST00000339598.7:c.1713C>G	ENSP00000344521.3:p.Thr571=
ENST00000402415.7:c.1944C>G	ENSP00000383906.3:p.Thr648=
ENST00000403946.7:c.4014C>G	ENSP00000385255.3:p.Thr1338=
NM_001287489.1:c.4014C>G	NP_001274418.1:p.Thr1338=
NM_004802.3:c.1713C>G	NP_004793.2:p.Thr571=
NM_194248.2:c.4014C>G	NP_919224.1:p.Thr1338=
NM_194322.2:c.1944C>G	NP_919303.1:p.Thr648=
NM_194323.2:c.1713C>G	NP_919304.1:p.Thr571=
XM_005264644.2:c.3999C>G	XP_005264701.1:p.Thr1333=
XM_011533185.1:c.4059C>G	XP_011531487.1:p.Thr1353=
XM_017005338.1:c.3954C>G	XP_016860827.1:p.Thr1318=
NM_001287489.2:c.4014C>G	NP_001274418.1:p.Thr1338=
NM_004802.4:c.1713C>G	NP_004793.2:p.Thr571=
NM_194248.3:c.4014C>G MANE Select	NP_919224.1:p.Thr1338=
NM_194322.3:c.1944C>G	NP_919303.1:p.Thr648=
NM_194323.3:c.1713C>G MANE Plus Clinical	NP_919304.1:p.Thr571=