Canonical Allele Identifier: CA425207355

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26690093G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467225G>T , CM000664.2:g.26467225G>T	GRCh38
NC_000002.11:g.26690093G>T , CM000664.1:g.26690093G>T	GRCh37
NC_000002.10:g.26543597G>T	NCBI36
NG_009937.1:g.96474C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4236C>A MANE Select	ENSP00000272371.2:p.Pro1412=
ENST00000339598.8:c.1935C>A MANE Plus Clinical	ENSP00000344521.3:p.Pro645=
ENST00000402415.8:c.1995C>A	ENSP00000383906.4:p.Pro665=
ENST00000272371.6:c.4236C>A	ENSP00000272371.2:p.Pro1412=
ENST00000338581.10:c.1935C>A	ENSP00000345137.6:p.Pro645=
ENST00000339598.7:c.1935C>A	ENSP00000344521.3:p.Pro645=
ENST00000402415.7:c.2166C>A	ENSP00000383906.3:p.Pro722=
ENST00000403946.7:c.4236C>A	ENSP00000385255.3:p.Pro1412=
NM_001287489.1:c.4236C>A	NP_001274418.1:p.Pro1412=
NM_004802.3:c.1935C>A	NP_004793.2:p.Pro645=
NM_194248.2:c.4236C>A	NP_919224.1:p.Pro1412=
NM_194322.2:c.2166C>A	NP_919303.1:p.Pro722=
NM_194323.2:c.1935C>A	NP_919304.1:p.Pro645=
XM_005264644.2:c.4221C>A	XP_005264701.1:p.Pro1407=
XM_011533185.1:c.4281C>A	XP_011531487.1:p.Pro1427=
XM_017005338.1:c.4176C>A	XP_016860827.1:p.Pro1392=
NM_001287489.2:c.4236C>A	NP_001274418.1:p.Pro1412=
NM_004802.4:c.1935C>A	NP_004793.2:p.Pro645=
NM_194248.3:c.4236C>A MANE Select	NP_919224.1:p.Pro1412=
NM_194322.3:c.2166C>A	NP_919303.1:p.Pro722=
NM_194323.3:c.1935C>A MANE Plus Clinical	NP_919304.1:p.Pro645=