Canonical Allele Identifier: CA1563989

Gene: OTOF

Linked Data

• ClinVar Variation Id: 1955006
• ClinVar RCV Id: RCV002690364
• dbSNP Id: rs752514163
• ExAC: 2:26700566 G / T
• gnomAD v2: 2-26700566-G-T
• gnomAD v3: 2-26477698-G-T
• gnomAD v4: 2-26477698-G-T
• MyVariant Identifiers: chr2:g.26700566G>T (hg19) ; chr2:g.26477698G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26477698G>T , CM000664.2:g.26477698G>T	GRCh38
NC_000002.11:g.26700566G>T , CM000664.1:g.26700566G>T	GRCh37
NC_000002.10:g.26554070G>T	NCBI36
NG_009937.1:g.86001C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.2266C>A MANE Select	ENSP00000272371.2:p.Pro756Thr
ENST00000339598.8:c.25C>A MANE Plus Clinical	ENSP00000344521.3:p.Pro9Thr
ENST00000402415.8:c.25C>A	ENSP00000383906.4:p.Pro9Thr
ENST00000272371.6:c.2266C>A	ENSP00000272371.2:p.Pro756Thr
ENST00000338581.10:c.25C>A	ENSP00000345137.6:p.Pro9Thr
ENST00000339598.7:c.25C>A	ENSP00000344521.3:p.Pro9Thr
ENST00000402415.7:c.196C>A	ENSP00000383906.3:p.Pro66Thr
ENST00000403946.7:c.2266C>A	ENSP00000385255.3:p.Pro756Thr
NM_001287489.1:c.2266C>A	NP_001274418.1:p.Pro756Thr
NM_004802.3:c.25C>A	NP_004793.2:p.Pro9Thr
NM_194248.2:c.2266C>A	NP_919224.1:p.Pro756Thr
NM_194322.2:c.196C>A	NP_919303.1:p.Pro66Thr
NM_194323.2:c.25C>A	NP_919304.1:p.Pro9Thr
XM_005264644.2:c.2311C>A	XP_005264701.1:p.Pro771Thr
XM_011533185.1:c.2311C>A	XP_011531487.1:p.Pro771Thr
XM_017005338.1:c.2266C>A	XP_016860827.1:p.Pro756Thr
NM_001287489.2:c.2266C>A	NP_001274418.1:p.Pro756Thr
NM_004802.4:c.25C>A	NP_004793.2:p.Pro9Thr
NM_194248.3:c.2266C>A MANE Select	NP_919224.1:p.Pro756Thr
NM_194322.3:c.196C>A	NP_919303.1:p.Pro66Thr
NM_194323.3:c.25C>A MANE Plus Clinical	NP_919304.1:p.Pro9Thr