Canonical Allele Identifier: CA346137698

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26707363G>A (hg19) ; chr2:g.26484495G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26484495G>A , CM000664.2:g.26484495G>A	GRCh38
NC_000002.11:g.26707363G>A , CM000664.1:g.26707363G>A	GRCh37
NC_000002.10:g.26560867G>A	NCBI36
NG_009937.1:g.79204C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.1184C>T MANE Select	ENSP00000272371.2:p.Thr395Ile
ENST00000272371.6:c.1184C>T	ENSP00000272371.2:p.Thr395Ile
ENST00000403946.7:c.1184C>T	ENSP00000385255.3:p.Thr395Ile
NM_001287489.1:c.1184C>T	NP_001274418.1:p.Thr395Ile
NM_194248.2:c.1184C>T	NP_919224.1:p.Thr395Ile
XM_005264644.2:c.1229C>T	XP_005264701.1:p.Thr410Ile
XM_011533185.1:c.1229C>T	XP_011531487.1:p.Thr410Ile
XM_017005338.1:c.1184C>T	XP_016860827.1:p.Thr395Ile
NM_001287489.2:c.1184C>T	NP_001274418.1:p.Thr395Ile
NM_194248.3:c.1184C>T MANE Select	NP_919224.1:p.Thr395Ile