Canonical Allele Identifier: CA346127773

Gene: OTOF

Linked Data

• gnomAD v4: 2-26460139-G-C
• MyVariant Identifiers: chr2:g.26683007G>C (hg19) ; chr2:g.26460139G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460139G>C , CM000664.2:g.26460139G>C	GRCh38
NC_000002.11:g.26683007G>C , CM000664.1:g.26683007G>C	GRCh37
NC_000002.10:g.26536511G>C	NCBI36
NG_009937.1:g.103560C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.5880C>G MANE Select	ENSP00000272371.2:p.His1960Gln
ENST00000339598.8:c.3512+508C>G MANE Plus Clinical	ENSP00000344521.3:n.3512+508C>G
ENST00000402415.8:c.3639C>G	ENSP00000383906.4:p.His1213Gln
ENST00000272371.6:c.5880C>G	ENSP00000272371.2:p.His1960Gln
ENST00000338581.10:c.3579C>G	ENSP00000345137.6:p.His1193Gln
ENST00000339598.7:c.3512+508C>G	ENSP00000344521.3:n.3512+508C>G
ENST00000402415.7:c.3810C>G	ENSP00000383906.3:p.His1270Gln
ENST00000403946.7:c.5813+508C>G	ENSP00000385255.3:n.5813+508C>G
NM_001287489.1:c.5813+508C>G	NP_001274418.1:n.5813+508C>G
NM_004802.3:c.3579C>G	NP_004793.2:p.His1193Gln
NM_194248.2:c.5880C>G	NP_919224.1:p.His1960Gln
NM_194322.2:c.3810C>G	NP_919303.1:p.His1270Gln
NM_194323.2:c.3512+508C>G	NP_919304.1:n.3512+508C>G
XM_005264644.2:c.5798+508C>G	XP_005264701.1:n.5798+508C>G
XM_011533185.1:c.5858+508C>G	XP_011531487.1:n.5858+508C>G
XM_017005338.1:c.5820C>G	XP_016860827.1:p.His1940Gln
NM_001287489.2:c.5813+508C>G	NP_001274418.1:n.5813+508C>G
NM_004802.4:c.3579C>G	NP_004793.2:p.His1193Gln
NM_194248.3:c.5880C>G MANE Select	NP_919224.1:p.His1960Gln
NM_194322.3:c.3810C>G	NP_919303.1:p.His1270Gln
NM_194323.3:c.3512+508C>G MANE Plus Clinical	NP_919304.1:n.3512+508C>G