Canonical Allele Identifier: CA2632222481

Gene: OTOA

Linked Data

• gnomAD v4: 16-21736250-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21736250C>T , CM000678.2:g.21736250C>T	GRCh38
NC_000016.9:g.21747571C>T , CM000678.1:g.21747571C>T	GRCh37
NC_000016.8:g.21655072C>T	NCBI36
NG_012973.1:g.62737C>T
NG_012973.2:g.77118C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000388958.8:c.2302-11C>T	ENSP00000373610.3:n.2302-11C>T
ENST00000646100.2:c.2302-11C>T MANE Select	ENSP00000496564.2:n.2302-11C>T
ENST00000647277.1:c.*1116-11C>T	ENSP00000495594.1:n.*1116-11C>T
ENST00000286149.8:c.2344-11C>T	ENSP00000286149.4:n.2344-11C>T
ENST00000388956.8:c.2065-11C>T	ENSP00000373608.4:n.2065-11C>T
ENST00000388957.3:c.1330-11C>T	ENSP00000373609.3:n.1330-11C>T
ENST00000388958.7:c.2302-11C>T	ENSP00000373610.3:n.2302-11C>T
ENST00000563506.1:n.1361-11C>T
ENST00000563871.5:n.1765-11C>T
NM_001161683.1:c.2065-11C>T	NP_001155155.1:n.2065-11C>T
NM_144672.3:c.2302-11C>T	NP_653273.3:n.2302-11C>T
NM_170664.2:c.1330-11C>T	NP_733764.1:n.1330-11C>T
XM_011545747.1:c.2302-11C>T	XP_011544049.1:n.2302-11C>T
XM_011545748.1:c.1171-11C>T	XP_011544050.1:n.1171-11C>T
NM_144672.4:c.2302-11C>T MANE Select	NP_653273.3:n.2302-11C>T
XM_011545748.2:c.1171-11C>T	XP_011544050.2:n.1171-11C>T
XM_017022951.1:c.568-11C>T	XP_016878440.1:n.568-11C>T
XR_002957775.1:n.1397-11C>T
NM_001161683.2:c.2065-11C>T	NP_001155155.1:n.2065-11C>T
NM_170664.3:c.1330-11C>T	NP_733764.1:n.1330-11C>T