Canonical Allele Identifier: CA1239827956

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26481025_26481026delinsCA , CM000664.2:g.26481025_26481026delinsCA	GRCh38
NC_000002.11:g.26703893_26703894delinsCA , CM000664.1:g.26703893_26703894delinsCA	GRCh37
NC_000002.10:g.26557397_26557398delinsCA	NCBI36
NG_009937.1:g.82673_82674delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1580-17_1580-16delinsTG MANE Select	ENSP00000272371.2:n.1580-17_1580-16delinsTG
ENST00000272371.6:c.1580-17_1580-16delinsTG	ENSP00000272371.2:n.1580-17_1580-16delinsTG
ENST00000403946.7:c.1580-17_1580-16delinsTG	ENSP00000385255.3:n.1580-17_1580-16delinsTG
NM_001287489.1:c.1580-17_1580-16delinsTG	NP_001274418.1:n.1580-17_1580-16delinsTG
NM_194248.2:c.1580-17_1580-16delinsTG	NP_919224.1:n.1580-17_1580-16delinsTG
XM_005264644.2:c.1625-17_1625-16delinsTG	XP_005264701.1:n.1625-17_1625-16delinsTG
XM_011533185.1:c.1625-17_1625-16delinsTG	XP_011531487.1:n.1625-17_1625-16delinsTG
XM_017005338.1:c.1580-17_1580-16delinsTG	XP_016860827.1:n.1580-17_1580-16delinsTG
NM_001287489.2:c.1580-17_1580-16delinsTG	NP_001274418.1:n.1580-17_1580-16delinsTG
NM_194248.3:c.1580-17_1580-16delinsTG MANE Select	NP_919224.1:n.1580-17_1580-16delinsTG