Canonical Allele Identifier: CA621292629

Gene: OTOA

Linked Data

• dbSNP Id: rs1567400115
• gnomAD v2: 16-21747574-T-C
• gnomAD v4: 16-21736253-T-C
• MyVariant Identifiers: chr16:g.21747574_21747576delinsCCA (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21736253T>C , CM000678.2:g.21736253T>C	GRCh38
NC_000016.9:g.21747574T>C , CM000678.1:g.21747574T>C	GRCh37
NC_000016.8:g.21655075T>C	NCBI36
NG_012973.1:g.62740T>C
NG_012973.2:g.77121T>C

Transcript Alleles

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