Canonical Allele Identifier: CA425359903

Gene: OTOF

Linked Data

• ClinVar Variation Id: 2830225
• ClinVar RCV Id: RCV003694151
• dbSNP Id: rs748585019
• MyVariant Identifiers: chr2:g.26698809G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26475941G>A , CM000664.2:g.26475941G>A	GRCh38
NC_000002.11:g.26698809G>A , CM000664.1:g.26698809G>A	GRCh37
NC_000002.10:g.26552313G>A	NCBI36
NG_009937.1:g.87758C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.2964C>T MANE Select	ENSP00000272371.2:p.Phe988=
ENST00000339598.8:c.723C>T MANE Plus Clinical	ENSP00000344521.3:p.Phe241=
ENST00000402415.8:c.723C>T	ENSP00000383906.4:p.Phe241=
ENST00000272371.6:c.2964C>T	ENSP00000272371.2:p.Phe988=
ENST00000338581.10:c.723C>T	ENSP00000345137.6:p.Phe241=
ENST00000339598.7:c.723C>T	ENSP00000344521.3:p.Phe241=
ENST00000402415.7:c.894C>T	ENSP00000383906.3:p.Phe298=
ENST00000403946.7:c.2964C>T	ENSP00000385255.3:p.Phe988=
NM_001287489.1:c.2964C>T	NP_001274418.1:p.Phe988=
NM_004802.3:c.723C>T	NP_004793.2:p.Phe241=
NM_194248.2:c.2964C>T	NP_919224.1:p.Phe988=
NM_194322.2:c.894C>T	NP_919303.1:p.Phe298=
NM_194323.2:c.723C>T	NP_919304.1:p.Phe241=
XM_005264644.2:c.3009C>T	XP_005264701.1:p.Phe1003=
XM_011533185.1:c.3009C>T	XP_011531487.1:p.Phe1003=
XM_017005338.1:c.2964C>T	XP_016860827.1:p.Phe988=
NM_001287489.2:c.2964C>T	NP_001274418.1:p.Phe988=
NM_004802.4:c.723C>T	NP_004793.2:p.Phe241=
NM_194248.3:c.2964C>T MANE Select	NP_919224.1:p.Phe988=
NM_194322.3:c.894C>T	NP_919303.1:p.Phe298=
NM_194323.3:c.723C>T MANE Plus Clinical	NP_919304.1:p.Phe241=