Canonical Allele Identifier: CA346137246

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26690263C>G (hg19) ; chr2:g.26467395C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467395C>G , CM000664.2:g.26467395C>G	GRCh38
NC_000002.11:g.26690263C>G , CM000664.1:g.26690263C>G	GRCh37
NC_000002.10:g.26543767C>G	NCBI36
NG_009937.1:g.96304G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4197G>C MANE Select	ENSP00000272371.2:p.Glu1399Asp
ENST00000339598.8:c.1896G>C MANE Plus Clinical	ENSP00000344521.3:p.Glu632Asp
ENST00000402415.8:c.1956G>C	ENSP00000383906.4:p.Glu652Asp
ENST00000272371.6:c.4197G>C	ENSP00000272371.2:p.Glu1399Asp
ENST00000338581.10:c.1896G>C	ENSP00000345137.6:p.Glu632Asp
ENST00000339598.7:c.1896G>C	ENSP00000344521.3:p.Glu632Asp
ENST00000402415.7:c.2127G>C	ENSP00000383906.3:p.Glu709Asp
ENST00000403946.7:c.4197G>C	ENSP00000385255.3:p.Glu1399Asp
NM_001287489.1:c.4197G>C	NP_001274418.1:p.Glu1399Asp
NM_004802.3:c.1896G>C	NP_004793.2:p.Glu632Asp
NM_194248.2:c.4197G>C	NP_919224.1:p.Glu1399Asp
NM_194322.2:c.2127G>C	NP_919303.1:p.Glu709Asp
NM_194323.2:c.1896G>C	NP_919304.1:p.Glu632Asp
XM_005264644.2:c.4182G>C	XP_005264701.1:p.Glu1394Asp
XM_011533185.1:c.4242G>C	XP_011531487.1:p.Glu1414Asp
XM_017005338.1:c.4137G>C	XP_016860827.1:p.Glu1379Asp
NM_001287489.2:c.4197G>C	NP_001274418.1:p.Glu1399Asp
NM_004802.4:c.1896G>C	NP_004793.2:p.Glu632Asp
NM_194248.3:c.4197G>C MANE Select	NP_919224.1:p.Glu1399Asp
NM_194322.3:c.2127G>C	NP_919303.1:p.Glu709Asp
NM_194323.3:c.1896G>C MANE Plus Clinical	NP_919304.1:p.Glu632Asp