Canonical Allele Identifier: CA346136692

Gene: OTOF

Linked Data

• dbSNP Id: rs1274464930
• gnomAD v4: 2-26467098-C-T
• MyVariant Identifiers: chr2:g.26689966C>T (hg19) ; chr2:g.26467098C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26467098C>T , CM000664.2:g.26467098C>T	GRCh38
NC_000002.11:g.26689966C>T , CM000664.1:g.26689966C>T	GRCh37
NC_000002.10:g.26543470C>T	NCBI36
NG_009937.1:g.96601G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.4362+1G>A MANE Select	ENSP00000272371.2:n.4362+1G>A
ENST00000339598.8:c.2061+1G>A MANE Plus Clinical	ENSP00000344521.3:n.2061+1G>A
ENST00000402415.8:c.2121+1G>A	ENSP00000383906.4:n.2121+1G>A
ENST00000272371.6:c.4362+1G>A	ENSP00000272371.2:n.4362+1G>A
ENST00000338581.10:c.2061+1G>A	ENSP00000345137.6:n.2061+1G>A
ENST00000339598.7:c.2061+1G>A	ENSP00000344521.3:n.2061+1G>A
ENST00000402415.7:c.2292+1G>A	ENSP00000383906.3:n.2292+1G>A
ENST00000403946.7:c.4362+1G>A	ENSP00000385255.3:n.4362+1G>A
NM_001287489.1:c.4362+1G>A	NP_001274418.1:n.4362+1G>A
NM_004802.3:c.2061+1G>A	NP_004793.2:n.2061+1G>A
NM_194248.2:c.4362+1G>A	NP_919224.1:n.4362+1G>A
NM_194322.2:c.2292+1G>A	NP_919303.1:n.2292+1G>A
NM_194323.2:c.2061+1G>A	NP_919304.1:n.2061+1G>A
XM_005264644.2:c.4347+1G>A	XP_005264701.1:n.4347+1G>A
XM_011533185.1:c.4407+1G>A	XP_011531487.1:n.4407+1G>A
XM_017005338.1:c.4302+1G>A	XP_016860827.1:n.4302+1G>A
NM_001287489.2:c.4362+1G>A	NP_001274418.1:n.4362+1G>A
NM_004802.4:c.2061+1G>A	NP_004793.2:n.2061+1G>A
NM_194248.3:c.4362+1G>A MANE Select	NP_919224.1:n.4362+1G>A
NM_194322.3:c.2292+1G>A	NP_919303.1:n.2292+1G>A
NM_194323.3:c.2061+1G>A MANE Plus Clinical	NP_919304.1:n.2061+1G>A