Canonical Allele Identifier: CA2658233685

Gene: OTOF

Linked Data

• gnomAD v4: 2-26463932-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.26463932A>G , CM000664.2:g.26463932A>G	GRCh38
NC_000002.11:g.26686800A>G , CM000664.1:g.26686800A>G	GRCh37
NC_000002.10:g.26540304A>G	NCBI36
NG_009937.1:g.99767T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000272371.7:c.5103+32T>C MANE Select	ENSP00000272371.2:n.5103+32T>C
ENST00000339598.8:c.2802+32T>C MANE Plus Clinical	ENSP00000344521.3:n.2802+32T>C
ENST00000402415.8:c.2862+32T>C	ENSP00000383906.4:n.2862+32T>C
ENST00000272371.6:c.5103+32T>C	ENSP00000272371.2:n.5103+32T>C
ENST00000338581.10:c.2802+32T>C	ENSP00000345137.6:n.2802+32T>C
ENST00000339598.7:c.2802+32T>C	ENSP00000344521.3:n.2802+32T>C
ENST00000402415.7:c.3033+32T>C	ENSP00000383906.3:n.3033+32T>C
ENST00000403946.7:c.5103+32T>C	ENSP00000385255.3:n.5103+32T>C
ENST00000464574.1:n.852+32T>C
NM_001287489.1:c.5103+32T>C	NP_001274418.1:n.5103+32T>C
NM_004802.3:c.2802+32T>C	NP_004793.2:n.2802+32T>C
NM_194248.2:c.5103+32T>C	NP_919224.1:n.5103+32T>C
NM_194322.2:c.3033+32T>C	NP_919303.1:n.3033+32T>C
NM_194323.2:c.2802+32T>C	NP_919304.1:n.2802+32T>C
XM_005264644.2:c.5088+32T>C	XP_005264701.1:n.5088+32T>C
XM_011533185.1:c.5148+32T>C	XP_011531487.1:n.5148+32T>C
XM_017005338.1:c.5043+32T>C	XP_016860827.1:n.5043+32T>C
NM_001287489.2:c.5103+32T>C	NP_001274418.1:n.5103+32T>C
NM_004802.4:c.2802+32T>C	NP_004793.2:n.2802+32T>C
NM_194248.3:c.5103+32T>C MANE Select	NP_919224.1:n.5103+32T>C
NM_194322.3:c.3033+32T>C	NP_919303.1:n.3033+32T>C
NM_194323.3:c.2802+32T>C MANE Plus Clinical	NP_919304.1:n.2802+32T>C