Canonical Allele Identifier: CA1239826972

Gene: OTOF

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26479988T= , CM000664.2:g.26479988T=	GRCh38
NC_000002.11:g.26702856T= , CM000664.1:g.26702856T=	GRCh37
NC_000002.10:g.26556360T=	NCBI36
NG_009937.1:g.83711A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1912+215A= MANE Select	ENSP00000272371.2:n.1912+215A=
ENST00000272371.6:c.1912+215A=	ENSP00000272371.2:n.1912+215A=
ENST00000403946.7:c.1912+215A=	ENSP00000385255.3:n.1912+215A=
NM_001287489.1:c.1912+215A=	NP_001274418.1:n.1912+215A=
NM_194248.2:c.1912+215A=	NP_919224.1:n.1912+215A=
XM_005264644.2:c.1957+215A=	XP_005264701.1:n.1957+215A=
XM_011533185.1:c.1957+215A=	XP_011531487.1:n.1957+215A=
XM_017005338.1:c.1912+215A=	XP_016860827.1:n.1912+215A=
NM_001287489.2:c.1912+215A=	NP_001274418.1:n.1912+215A=
NM_194248.3:c.1912+215A= MANE Select	NP_919224.1:n.1912+215A=