Canonical Allele Identifier: CA346137697

Gene: OTOF

Linked Data

• gnomAD v4: 2-26484495-G-C
• MyVariant Identifiers: chr2:g.26707363G>C (hg19) ; chr2:g.26484495G>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.1184C>G MANE Select	ENSP00000272371.2:p.Thr395Ser
ENST00000272371.6:c.1184C>G	ENSP00000272371.2:p.Thr395Ser
ENST00000403946.7:c.1184C>G	ENSP00000385255.3:p.Thr395Ser
NM_001287489.1:c.1184C>G	NP_001274418.1:p.Thr395Ser
NM_194248.2:c.1184C>G	NP_919224.1:p.Thr395Ser
XM_005264644.2:c.1229C>G	XP_005264701.1:p.Thr410Ser
XM_011533185.1:c.1229C>G	XP_011531487.1:p.Thr410Ser
XM_017005338.1:c.1184C>G	XP_016860827.1:p.Thr395Ser
NM_001287489.2:c.1184C>G	NP_001274418.1:p.Thr395Ser
NM_194248.3:c.1184C>G MANE Select	NP_919224.1:p.Thr395Ser