Canonical Allele Identifier: CA1562665

Gene: OTOF

Linked Data

• ClinVar Variation Id: 3017824
• ClinVar RCV Id: RCV003874423
• dbSNP Id: rs370716879
• ExAC: 2:26683004 C / T
• gnomAD v2: 2-26683004-C-T
• gnomAD v4: 2-26460136-C-T
• MyVariant Identifiers: chr2:g.26683004C>T (hg19) ; chr2:g.26460136C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460136C>T , CM000664.2:g.26460136C>T	GRCh38
NC_000002.11:g.26683004C>T , CM000664.1:g.26683004C>T	GRCh37
NC_000002.10:g.26536508C>T	NCBI36
NG_009937.1:g.103563G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5883G>A MANE Select	ENSP00000272371.2:p.Thr1961=
ENST00000339598.8:c.3512+511G>A MANE Plus Clinical	ENSP00000344521.3:n.3512+511G>A
ENST00000402415.8:c.3642G>A	ENSP00000383906.4:p.Thr1214=
ENST00000272371.6:c.5883G>A	ENSP00000272371.2:p.Thr1961=
ENST00000338581.10:c.3582G>A	ENSP00000345137.6:p.Thr1194=
ENST00000339598.7:c.3512+511G>A	ENSP00000344521.3:n.3512+511G>A
ENST00000402415.7:c.3813G>A	ENSP00000383906.3:p.Thr1271=
ENST00000403946.7:c.5813+511G>A	ENSP00000385255.3:n.5813+511G>A
NM_001287489.1:c.5813+511G>A	NP_001274418.1:n.5813+511G>A
NM_004802.3:c.3582G>A	NP_004793.2:p.Thr1194=
NM_194248.2:c.5883G>A	NP_919224.1:p.Thr1961=
NM_194322.2:c.3813G>A	NP_919303.1:p.Thr1271=
NM_194323.2:c.3512+511G>A	NP_919304.1:n.3512+511G>A
XM_005264644.2:c.5798+511G>A	XP_005264701.1:n.5798+511G>A
XM_011533185.1:c.5858+511G>A	XP_011531487.1:n.5858+511G>A
XM_017005338.1:c.5823G>A	XP_016860827.1:p.Thr1941=
NM_001287489.2:c.5813+511G>A	NP_001274418.1:n.5813+511G>A
NM_004802.4:c.3582G>A	NP_004793.2:p.Thr1194=
NM_194248.3:c.5883G>A MANE Select	NP_919224.1:p.Thr1961=
NM_194322.3:c.3813G>A	NP_919303.1:p.Thr1271=
NM_194323.3:c.3512+511G>A MANE Plus Clinical	NP_919304.1:n.3512+511G>A