Canonical Allele Identifier: CA7952942

Gene: OTOA

Linked Data

• dbSNP Id: rs753916852
• ExAC: 16:21747540 G / A
• gnomAD v2: 16-21747540-G-A
• gnomAD v4: 16-21736219-G-A
• MyVariant Identifiers: chr16:g.21747540G>A (hg19) ; chr16:g.21747540_21747541delinsAT (hg19) ; chr16:g.21736219G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21736219G>A , CM000678.2:g.21736219G>A	GRCh38
NC_000016.9:g.21747540G>A , CM000678.1:g.21747540G>A	GRCh37
NC_000016.8:g.21655041G>A	NCBI36
NG_012973.1:g.62706G>A
NG_012973.2:g.77087G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.2302-42G>A	ENSP00000373610.3:n.2302-42G>A
ENST00000646100.2:c.2302-42G>A MANE Select	ENSP00000496564.2:n.2302-42G>A
ENST00000647277.1:c.*1116-42G>A	ENSP00000495594.1:n.*1116-42G>A
ENST00000286149.8:c.2344-42G>A	ENSP00000286149.4:n.2344-42G>A
ENST00000388956.8:c.2065-42G>A	ENSP00000373608.4:n.2065-42G>A
ENST00000388957.3:c.1330-42G>A	ENSP00000373609.3:n.1330-42G>A
ENST00000388958.7:c.2302-42G>A	ENSP00000373610.3:n.2302-42G>A
ENST00000563506.1:n.1361-42G>A
ENST00000563871.5:n.1765-42G>A
NM_001161683.1:c.2065-42G>A	NP_001155155.1:n.2065-42G>A
NM_144672.3:c.2302-42G>A	NP_653273.3:n.2302-42G>A
NM_170664.2:c.1330-42G>A	NP_733764.1:n.1330-42G>A
XM_011545747.1:c.2302-42G>A	XP_011544049.1:n.2302-42G>A
XM_011545748.1:c.1171-42G>A	XP_011544050.1:n.1171-42G>A
NM_144672.4:c.2302-42G>A MANE Select	NP_653273.3:n.2302-42G>A
XM_011545748.2:c.1171-42G>A	XP_011544050.2:n.1171-42G>A
XM_017022951.1:c.568-42G>A	XP_016878440.1:n.568-42G>A
XR_002957775.1:n.1397-42G>A
NM_001161683.2:c.2065-42G>A	NP_001155155.1:n.2065-42G>A
NM_170664.3:c.1330-42G>A	NP_733764.1:n.1330-42G>A