Canonical Allele Identifier: CA346133654

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26686834G>C (hg19) ; chr2:g.26463966G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26463966G>C , CM000664.2:g.26463966G>C	GRCh38
NC_000002.11:g.26686834G>C , CM000664.1:g.26686834G>C	GRCh37
NC_000002.10:g.26540338G>C	NCBI36
NG_009937.1:g.99733C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.5101C>G MANE Select	ENSP00000272371.2:p.Gln1701Glu
ENST00000339598.8:c.2800C>G MANE Plus Clinical	ENSP00000344521.3:p.Gln934Glu
ENST00000402415.8:c.2860C>G	ENSP00000383906.4:p.Gln954Glu
ENST00000272371.6:c.5101C>G	ENSP00000272371.2:p.Gln1701Glu
ENST00000338581.10:c.2800C>G	ENSP00000345137.6:p.Gln934Glu
ENST00000339598.7:c.2800C>G	ENSP00000344521.3:p.Gln934Glu
ENST00000402415.7:c.3031C>G	ENSP00000383906.3:p.Gln1011Glu
ENST00000403946.7:c.5101C>G	ENSP00000385255.3:p.Gln1701Glu
ENST00000464574.1:n.850C>G
NM_001287489.1:c.5101C>G	NP_001274418.1:p.Gln1701Glu
NM_004802.3:c.2800C>G	NP_004793.2:p.Gln934Glu
NM_194248.2:c.5101C>G	NP_919224.1:p.Gln1701Glu
NM_194322.2:c.3031C>G	NP_919303.1:p.Gln1011Glu
NM_194323.2:c.2800C>G	NP_919304.1:p.Gln934Glu
XM_005264644.2:c.5086C>G	XP_005264701.1:p.Gln1696Glu
XM_011533185.1:c.5146C>G	XP_011531487.1:p.Gln1716Glu
XM_017005338.1:c.5041C>G	XP_016860827.1:p.Gln1681Glu
NM_001287489.2:c.5101C>G	NP_001274418.1:p.Gln1701Glu
NM_004802.4:c.2800C>G	NP_004793.2:p.Gln934Glu
NM_194248.3:c.5101C>G MANE Select	NP_919224.1:p.Gln1701Glu
NM_194322.3:c.3031C>G	NP_919303.1:p.Gln1011Glu
NM_194323.3:c.2800C>G MANE Plus Clinical	NP_919304.1:p.Gln934Glu