Canonical Allele Identifier: CA2739274215

Gene: OTOF

Linked Data

• ClinVar Variation Id: 2825972
• ClinVar RCV Id: RCV003681203

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26470424_26470691delinsC , CM000664.2:g.26470424_26470691delinsC	GRCh38
NC_000002.11:g.26693292_26693559delinsC , CM000664.1:g.26693292_26693559delinsC	GRCh37
NC_000002.10:g.26546796_26547063delinsC	NCBI36
NG_009937.1:g.93008_93275delinsG

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.3925_4023+169delinsG
ENST00000339598.8:c.1624_1722+169delinsG
ENST00000402415.8:c.1684_1782+169delinsG
ENST00000272371.6:c.3925_4023+169delinsG
ENST00000338581.10:c.1624_1722+169delinsG
ENST00000339598.7:c.1624_1722+169delinsG
ENST00000402415.7:c.1855_1953+169delinsG
ENST00000403946.7:c.3925_4023+169delinsG
NM_001287489.1:c.3925_4023+169delinsG
NM_004802.3:c.1624_1722+169delinsG
NM_194248.2:c.3925_4023+169delinsG
NM_194322.2:c.1855_1953+169delinsG
NM_194323.2:c.1624_1722+169delinsG
XM_005264644.2:c.3910_4008+169delinsG
XM_011533185.1:c.3970_4068+169delinsG
XM_017005338.1:c.3865_3963+169delinsG
NM_001287489.2:c.3925_4023+169delinsG
NM_004802.4:c.1624_1722+169delinsG
NM_194248.3:c.3925_4023+169delinsG
NM_194322.3:c.1855_1953+169delinsG
NM_194323.3:c.1624_1722+169delinsG