Canonical Allele Identifier: CA425207021

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26706393A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26483525A>C , CM000664.2:g.26483525A>C	GRCh38
NC_000002.11:g.26706393A>C , CM000664.1:g.26706393A>C	GRCh37
NC_000002.10:g.26559897A>C	NCBI36
NG_009937.1:g.80174T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000272371.7:c.1329T>G MANE Select	ENSP00000272371.2:p.Ala443=
ENST00000272371.6:c.1329T>G	ENSP00000272371.2:p.Ala443=
ENST00000403946.7:c.1329T>G	ENSP00000385255.3:p.Ala443=
NM_001287489.1:c.1329T>G	NP_001274418.1:p.Ala443=
NM_194248.2:c.1329T>G	NP_919224.1:p.Ala443=
XM_005264644.2:c.1374T>G	XP_005264701.1:p.Ala458=
XM_011533185.1:c.1374T>G	XP_011531487.1:p.Ala458=
XM_017005338.1:c.1329T>G	XP_016860827.1:p.Ala443=
NM_001287489.2:c.1329T>G	NP_001274418.1:p.Ala443=
NM_194248.3:c.1329T>G MANE Select	NP_919224.1:p.Ala443=