Canonical Allele Identifier: CA346137065

Gene: OTOF

Linked Data

• dbSNP Id: rs1664774258
• gnomAD v3: 2-26467213-C-A
• gnomAD v4: 2-26467213-C-A
• MyVariant Identifiers: chr2:g.26690081C>A (hg19) ; chr2:g.26467213C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467213C>A , CM000664.2:g.26467213C>A	GRCh38
NC_000002.11:g.26690081C>A , CM000664.1:g.26690081C>A	GRCh37
NC_000002.10:g.26543585C>A	NCBI36
NG_009937.1:g.96486G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4248G>T MANE Select	ENSP00000272371.2:p.Glu1416Asp
ENST00000339598.8:c.1947G>T MANE Plus Clinical	ENSP00000344521.3:p.Glu649Asp
ENST00000402415.8:c.2007G>T	ENSP00000383906.4:p.Glu669Asp
ENST00000272371.6:c.4248G>T	ENSP00000272371.2:p.Glu1416Asp
ENST00000338581.10:c.1947G>T	ENSP00000345137.6:p.Glu649Asp
ENST00000339598.7:c.1947G>T	ENSP00000344521.3:p.Glu649Asp
ENST00000402415.7:c.2178G>T	ENSP00000383906.3:p.Glu726Asp
ENST00000403946.7:c.4248G>T	ENSP00000385255.3:p.Glu1416Asp
NM_001287489.1:c.4248G>T	NP_001274418.1:p.Glu1416Asp
NM_004802.3:c.1947G>T	NP_004793.2:p.Glu649Asp
NM_194248.2:c.4248G>T	NP_919224.1:p.Glu1416Asp
NM_194322.2:c.2178G>T	NP_919303.1:p.Glu726Asp
NM_194323.2:c.1947G>T	NP_919304.1:p.Glu649Asp
XM_005264644.2:c.4233G>T	XP_005264701.1:p.Glu1411Asp
XM_011533185.1:c.4293G>T	XP_011531487.1:p.Glu1431Asp
XM_017005338.1:c.4188G>T	XP_016860827.1:p.Glu1396Asp
NM_001287489.2:c.4248G>T	NP_001274418.1:p.Glu1416Asp
NM_004802.4:c.1947G>T	NP_004793.2:p.Glu649Asp
NM_194248.3:c.4248G>T MANE Select	NP_919224.1:p.Glu1416Asp
NM_194322.3:c.2178G>T	NP_919303.1:p.Glu726Asp
NM_194323.3:c.1947G>T MANE Plus Clinical	NP_919304.1:p.Glu649Asp