Canonical Allele Identifier: CA1239827400

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26480480_26480482delinsCAT , CM000664.2:g.26480480_26480482delinsCAT	GRCh38
NC_000002.11:g.26703348_26703350delinsCAT , CM000664.1:g.26703348_26703350delinsCAT	GRCh37
NC_000002.10:g.26556852_26556854delinsCAT	NCBI36
NG_009937.1:g.83217_83219delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1804-171_1804-169delinsATG MANE Select	ENSP00000272371.2:n.1804-171_1804-169delinsATG
ENST00000272371.6:c.1804-171_1804-169delinsATG	ENSP00000272371.2:n.1804-171_1804-169delinsATG
ENST00000403946.7:c.1804-171_1804-169delinsATG	ENSP00000385255.3:n.1804-171_1804-169delinsATG
NM_001287489.1:c.1804-171_1804-169delinsATG	NP_001274418.1:n.1804-171_1804-169delinsATG
NM_194248.2:c.1804-171_1804-169delinsATG	NP_919224.1:n.1804-171_1804-169delinsATG
XM_005264644.2:c.1849-171_1849-169delinsATG	XP_005264701.1:n.1849-171_1849-169delinsATG
XM_011533185.1:c.1849-171_1849-169delinsATG	XP_011531487.1:n.1849-171_1849-169delinsATG
XM_017005338.1:c.1804-171_1804-169delinsATG	XP_016860827.1:n.1804-171_1804-169delinsATG
NM_001287489.2:c.1804-171_1804-169delinsATG	NP_001274418.1:n.1804-171_1804-169delinsATG
NM_194248.3:c.1804-171_1804-169delinsATG MANE Select	NP_919224.1:n.1804-171_1804-169delinsATG