Canonical Allele Identifier: CA346127419

Gene: OTOF

Linked Data

• MyVariant Identifiers: chr2:g.26682921T>G (hg19) ; chr2:g.26460053T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26460053T>G , CM000664.2:g.26460053T>G	GRCh38
NC_000002.11:g.26682921T>G , CM000664.1:g.26682921T>G	GRCh37
NC_000002.10:g.26536425T>G	NCBI36
NG_009937.1:g.103646A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.5966A>C MANE Select	ENSP00000272371.2:p.Tyr1989Ser
ENST00000339598.8:c.3512+594A>C MANE Plus Clinical	ENSP00000344521.3:n.3512+594A>C
ENST00000402415.8:c.3725A>C	ENSP00000383906.4:p.Tyr1242Ser
ENST00000272371.6:c.5966A>C	ENSP00000272371.2:p.Tyr1989Ser
ENST00000338581.10:c.3665A>C	ENSP00000345137.6:p.Tyr1222Ser
ENST00000339598.7:c.3512+594A>C	ENSP00000344521.3:n.3512+594A>C
ENST00000402415.7:c.3896A>C	ENSP00000383906.3:p.Tyr1299Ser
ENST00000403946.7:c.5813+594A>C	ENSP00000385255.3:n.5813+594A>C
NM_001287489.1:c.5813+594A>C	NP_001274418.1:n.5813+594A>C
NM_004802.3:c.3665A>C	NP_004793.2:p.Tyr1222Ser
NM_194248.2:c.5966A>C	NP_919224.1:p.Tyr1989Ser
NM_194322.2:c.3896A>C	NP_919303.1:p.Tyr1299Ser
NM_194323.2:c.3512+594A>C	NP_919304.1:n.3512+594A>C
XM_005264644.2:c.5798+594A>C	XP_005264701.1:n.5798+594A>C
XM_011533185.1:c.5858+594A>C	XP_011531487.1:n.5858+594A>C
XM_017005338.1:c.5906A>C	XP_016860827.1:p.Tyr1969Ser
NM_001287489.2:c.5813+594A>C	NP_001274418.1:n.5813+594A>C
NM_004802.4:c.3665A>C	NP_004793.2:p.Tyr1222Ser
NM_194248.3:c.5966A>C MANE Select	NP_919224.1:p.Tyr1989Ser
NM_194322.3:c.3896A>C	NP_919303.1:p.Tyr1299Ser
NM_194323.3:c.3512+594A>C MANE Plus Clinical	NP_919304.1:n.3512+594A>C