Canonical Allele Identifier: CA346131389

Gene: OTOF

Linked Data

• dbSNP Id: rs1664474751
• gnomAD v3: 2-26461764-T-C
• gnomAD v4: 2-26461764-T-C
• MyVariant Identifiers: chr2:g.26684632T>C (hg19) ; chr2:g.26461764T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26461764T>C , CM000664.2:g.26461764T>C	GRCh38
NC_000002.11:g.26684632T>C , CM000664.1:g.26684632T>C	GRCh37
NC_000002.10:g.26538136T>C	NCBI36
NG_009937.1:g.101935A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5465A>G MANE Select	ENSP00000272371.2:p.Tyr1822Cys
ENST00000339598.8:c.3164A>G MANE Plus Clinical	ENSP00000344521.3:p.Tyr1055Cys
ENST00000402415.8:c.3224A>G	ENSP00000383906.4:p.Tyr1075Cys
ENST00000272371.6:c.5465A>G	ENSP00000272371.2:p.Tyr1822Cys
ENST00000338581.10:c.3164A>G	ENSP00000345137.6:p.Tyr1055Cys
ENST00000339598.7:c.3164A>G	ENSP00000344521.3:p.Tyr1055Cys
ENST00000402415.7:c.3395A>G	ENSP00000383906.3:p.Tyr1132Cys
ENST00000403946.7:c.5465A>G	ENSP00000385255.3:p.Tyr1822Cys
NM_001287489.1:c.5465A>G	NP_001274418.1:p.Tyr1822Cys
NM_004802.3:c.3164A>G	NP_004793.2:p.Tyr1055Cys
NM_194248.2:c.5465A>G	NP_919224.1:p.Tyr1822Cys
NM_194322.2:c.3395A>G	NP_919303.1:p.Tyr1132Cys
NM_194323.2:c.3164A>G	NP_919304.1:p.Tyr1055Cys
XM_005264644.2:c.5450A>G	XP_005264701.1:p.Tyr1817Cys
XM_011533185.1:c.5510A>G	XP_011531487.1:p.Tyr1837Cys
XM_017005338.1:c.5405A>G	XP_016860827.1:p.Tyr1802Cys
NM_001287489.2:c.5465A>G	NP_001274418.1:p.Tyr1822Cys
NM_004802.4:c.3164A>G	NP_004793.2:p.Tyr1055Cys
NM_194248.3:c.5465A>G MANE Select	NP_919224.1:p.Tyr1822Cys
NM_194322.3:c.3395A>G	NP_919303.1:p.Tyr1132Cys
NM_194323.3:c.3164A>G MANE Plus Clinical	NP_919304.1:p.Tyr1055Cys