Canonical Allele Identifier: CA346127731

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26683000G>C (hg19) ; chr2:g.26460132G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460132G>C , CM000664.2:g.26460132G>C	GRCh38
NC_000002.11:g.26683000G>C , CM000664.1:g.26683000G>C	GRCh37
NC_000002.10:g.26536504G>C	NCBI36
NG_009937.1:g.103567C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5887C>G MANE Select	ENSP00000272371.2:p.Arg1963Gly
ENST00000339598.8:c.3512+515C>G MANE Plus Clinical	ENSP00000344521.3:n.3512+515C>G
ENST00000402415.8:c.3646C>G	ENSP00000383906.4:p.Arg1216Gly
ENST00000272371.6:c.5887C>G	ENSP00000272371.2:p.Arg1963Gly
ENST00000338581.10:c.3586C>G	ENSP00000345137.6:p.Arg1196Gly
ENST00000339598.7:c.3512+515C>G	ENSP00000344521.3:n.3512+515C>G
ENST00000402415.7:c.3817C>G	ENSP00000383906.3:p.Arg1273Gly
ENST00000403946.7:c.5813+515C>G	ENSP00000385255.3:n.5813+515C>G
NM_001287489.1:c.5813+515C>G	NP_001274418.1:n.5813+515C>G
NM_004802.3:c.3586C>G	NP_004793.2:p.Arg1196Gly
NM_194248.2:c.5887C>G	NP_919224.1:p.Arg1963Gly
NM_194322.2:c.3817C>G	NP_919303.1:p.Arg1273Gly
NM_194323.2:c.3512+515C>G	NP_919304.1:n.3512+515C>G
XM_005264644.2:c.5798+515C>G	XP_005264701.1:n.5798+515C>G
XM_011533185.1:c.5858+515C>G	XP_011531487.1:n.5858+515C>G
XM_017005338.1:c.5827C>G	XP_016860827.1:p.Arg1943Gly
NM_001287489.2:c.5813+515C>G	NP_001274418.1:n.5813+515C>G
NM_004802.4:c.3586C>G	NP_004793.2:p.Arg1196Gly
NM_194248.3:c.5887C>G MANE Select	NP_919224.1:p.Arg1963Gly
NM_194322.3:c.3817C>G	NP_919303.1:p.Arg1273Gly
NM_194323.3:c.3512+515C>G MANE Plus Clinical	NP_919304.1:n.3512+515C>G