Canonical Allele Identifier: CA346135372

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26705352C>A (hg19) ; chr2:g.26482484C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26482484C>A , CM000664.2:g.26482484C>A	GRCh38
NC_000002.11:g.26705352C>A , CM000664.1:g.26705352C>A	GRCh37
NC_000002.10:g.26558856C>A	NCBI36
NG_009937.1:g.81215G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.1501G>T MANE Select	ENSP00000272371.2:p.Asp501Tyr
ENST00000272371.6:c.1501G>T	ENSP00000272371.2:p.Asp501Tyr
ENST00000403946.7:c.1501G>T	ENSP00000385255.3:p.Asp501Tyr
NM_001287489.1:c.1501G>T	NP_001274418.1:p.Asp501Tyr
NM_194248.2:c.1501G>T	NP_919224.1:p.Asp501Tyr
XM_005264644.2:c.1546G>T	XP_005264701.1:p.Asp516Tyr
XM_011533185.1:c.1546G>T	XP_011531487.1:p.Asp516Tyr
XM_017005338.1:c.1501G>T	XP_016860827.1:p.Asp501Tyr
NM_001287489.2:c.1501G>T	NP_001274418.1:p.Asp501Tyr
NM_194248.3:c.1501G>T MANE Select	NP_919224.1:p.Asp501Tyr