Canonical Allele Identifier: CA346137293

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26690288G>C (hg19) ; chr2:g.26467420G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467420G>C , CM000664.2:g.26467420G>C	GRCh38
NC_000002.11:g.26690288G>C , CM000664.1:g.26690288G>C	GRCh37
NC_000002.10:g.26543792G>C	NCBI36
NG_009937.1:g.96279C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4172C>G MANE Select	ENSP00000272371.2:p.Ser1391Cys
ENST00000339598.8:c.1871C>G MANE Plus Clinical	ENSP00000344521.3:p.Ser624Cys
ENST00000402415.8:c.1931C>G	ENSP00000383906.4:p.Ser644Cys
ENST00000272371.6:c.4172C>G	ENSP00000272371.2:p.Ser1391Cys
ENST00000338581.10:c.1871C>G	ENSP00000345137.6:p.Ser624Cys
ENST00000339598.7:c.1871C>G	ENSP00000344521.3:p.Ser624Cys
ENST00000402415.7:c.2102C>G	ENSP00000383906.3:p.Ser701Cys
ENST00000403946.7:c.4172C>G	ENSP00000385255.3:p.Ser1391Cys
NM_001287489.1:c.4172C>G	NP_001274418.1:p.Ser1391Cys
NM_004802.3:c.1871C>G	NP_004793.2:p.Ser624Cys
NM_194248.2:c.4172C>G	NP_919224.1:p.Ser1391Cys
NM_194322.2:c.2102C>G	NP_919303.1:p.Ser701Cys
NM_194323.2:c.1871C>G	NP_919304.1:p.Ser624Cys
XM_005264644.2:c.4157C>G	XP_005264701.1:p.Ser1386Cys
XM_011533185.1:c.4217C>G	XP_011531487.1:p.Ser1406Cys
XM_017005338.1:c.4112C>G	XP_016860827.1:p.Ser1371Cys
NM_001287489.2:c.4172C>G	NP_001274418.1:p.Ser1391Cys
NM_004802.4:c.1871C>G	NP_004793.2:p.Ser624Cys
NM_194248.3:c.4172C>G MANE Select	NP_919224.1:p.Ser1391Cys
NM_194322.3:c.2102C>G	NP_919303.1:p.Ser701Cys
NM_194323.3:c.1871C>G MANE Plus Clinical	NP_919304.1:p.Ser624Cys