Canonical Allele Identifier: CA346124691

Gene: OTOF

Linked Data

• dbSNP Id: rs771364564
• gnomAD v2: 2-26700676-A-T
• gnomAD v4: 2-26477808-A-T
• MyVariant Identifiers: chr2:g.26700676A>T (hg19) ; chr2:g.26477808A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26477808A>T , CM000664.2:g.26477808A>T	GRCh38
NC_000002.11:g.26700676A>T , CM000664.1:g.26700676A>T	GRCh37
NC_000002.10:g.26554180A>T	NCBI36
NG_009937.1:g.85891T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.2215-59T>A MANE Select	ENSP00000272371.2:n.2215-59T>A
ENST00000339598.8:c.-28+36T>A MANE Plus Clinical	ENSP00000344521.3:n.-28+36T>A
ENST00000402415.8:c.-86T>A	ENSP00000383906.4:n.-86T>A
ENST00000272371.6:c.2215-59T>A	ENSP00000272371.2:n.2215-59T>A
ENST00000338581.10:c.-28+36T>A	ENSP00000345137.6:n.-28+36T>A
ENST00000339598.7:c.-28+36T>A	ENSP00000344521.3:n.-28+36T>A
ENST00000402415.7:c.86T>A	ENSP00000383906.3:p.Phe29Tyr
ENST00000403946.7:c.2215-59T>A	ENSP00000385255.3:n.2215-59T>A
NM_001287489.1:c.2215-59T>A	NP_001274418.1:n.2215-59T>A
NM_004802.3:c.-28+36T>A	NP_004793.2:n.-28+36T>A
NM_194248.2:c.2215-59T>A	NP_919224.1:n.2215-59T>A
NM_194322.2:c.86T>A	NP_919303.1:p.Phe29Tyr
NM_194323.2:c.-28+36T>A	NP_919304.1:n.-28+36T>A
XM_005264644.2:c.2260-59T>A	XP_005264701.1:n.2260-59T>A
XM_011533185.1:c.2260-59T>A	XP_011531487.1:n.2260-59T>A
XM_017005338.1:c.2215-59T>A	XP_016860827.1:n.2215-59T>A
NM_001287489.2:c.2215-59T>A	NP_001274418.1:n.2215-59T>A
NM_004802.4:c.-28+36T>A	NP_004793.2:n.-28+36T>A
NM_194248.3:c.2215-59T>A MANE Select	NP_919224.1:n.2215-59T>A
NM_194322.3:c.86T>A	NP_919303.1:p.Phe29Tyr
NM_194323.3:c.-28+36T>A MANE Plus Clinical	NP_919304.1:n.-28+36T>A