Canonical Allele Identifier: CA1239830002

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26477388A= , CM000664.2:g.26477388A=	GRCh38
NC_000002.11:g.26700256A= , CM000664.1:g.26700256A=	GRCh37
NC_000002.10:g.26553760A=	NCBI36
NG_009937.1:g.86311T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.2406+28T= MANE Select	ENSP00000272371.2:n.2406+28T=
ENST00000339598.8:c.165+28T= MANE Plus Clinical	ENSP00000344521.3:n.165+28T=
ENST00000402415.8:c.165+28T=	ENSP00000383906.4:n.165+28T=
ENST00000272371.6:c.2406+28T=	ENSP00000272371.2:n.2406+28T=
ENST00000338581.10:c.165+28T=	ENSP00000345137.6:n.165+28T=
ENST00000339598.7:c.165+28T=	ENSP00000344521.3:n.165+28T=
ENST00000402415.7:c.336+28T=	ENSP00000383906.3:n.336+28T=
ENST00000403946.7:c.2406+28T=	ENSP00000385255.3:n.2406+28T=
NM_001287489.1:c.2406+28T=	NP_001274418.1:n.2406+28T=
NM_004802.3:c.165+28T=	NP_004793.2:n.165+28T=
NM_194248.2:c.2406+28T=	NP_919224.1:n.2406+28T=
NM_194322.2:c.336+28T=	NP_919303.1:n.336+28T=
NM_194323.2:c.165+28T=	NP_919304.1:n.165+28T=
XM_005264644.2:c.2451+28T=	XP_005264701.1:n.2451+28T=
XM_011533185.1:c.2451+28T=	XP_011531487.1:n.2451+28T=
XM_017005338.1:c.2406+28T=	XP_016860827.1:n.2406+28T=
NM_001287489.2:c.2406+28T=	NP_001274418.1:n.2406+28T=
NM_004802.4:c.165+28T=	NP_004793.2:n.165+28T=
NM_194248.3:c.2406+28T= MANE Select	NP_919224.1:n.2406+28T=
NM_194322.3:c.336+28T=	NP_919303.1:n.336+28T=
NM_194323.3:c.165+28T= MANE Plus Clinical	NP_919304.1:n.165+28T=