Canonical Allele Identifier: CA1239826976

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26479990_26479991delinsGC , CM000664.2:g.26479990_26479991delinsGC	GRCh38
NC_000002.11:g.26702858_26702859delinsGC , CM000664.1:g.26702858_26702859delinsGC	GRCh37
NC_000002.10:g.26556362_26556363delinsGC	NCBI36
NG_009937.1:g.83708_83709delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1912+212_1912+213delinsGC MANE Select	ENSP00000272371.2:n.1912+212_1912+213delinsGC
ENST00000272371.6:c.1912+212_1912+213delinsGC	ENSP00000272371.2:n.1912+212_1912+213delinsGC
ENST00000403946.7:c.1912+212_1912+213delinsGC	ENSP00000385255.3:n.1912+212_1912+213delinsGC
NM_001287489.1:c.1912+212_1912+213delinsGC	NP_001274418.1:n.1912+212_1912+213delinsGC
NM_194248.2:c.1912+212_1912+213delinsGC	NP_919224.1:n.1912+212_1912+213delinsGC
XM_005264644.2:c.1957+212_1957+213delinsGC	XP_005264701.1:n.1957+212_1957+213delinsGC
XM_011533185.1:c.1957+212_1957+213delinsGC	XP_011531487.1:n.1957+212_1957+213delinsGC
XM_017005338.1:c.1912+212_1912+213delinsGC	XP_016860827.1:n.1912+212_1912+213delinsGC
NM_001287489.2:c.1912+212_1912+213delinsGC	NP_001274418.1:n.1912+212_1912+213delinsGC
NM_194248.3:c.1912+212_1912+213delinsGC MANE Select	NP_919224.1:n.1912+212_1912+213delinsGC