Canonical Allele Identifier: CA621300056

Gene: OTOA

Linked Data

• dbSNP Id: rs1423810972
• gnomAD v2: 16-21716462-C-T
• gnomAD v4: 16-21705141-C-T
• MyVariant Identifiers: chr16:g.21716462C>T (hg19) ; chr16:g.21705141C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21705141C>T , CM000678.2:g.21705141C>T	GRCh38
NC_000016.9:g.21716462C>T , CM000678.1:g.21716462C>T	GRCh37
NC_000016.8:g.21623963C>T	NCBI36
NG_012973.1:g.31628C>T
NG_012973.2:g.46009C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000388958.8:c.981-28C>T	ENSP00000373610.3:n.981-28C>T
ENST00000646100.2:c.981-28C>T MANE Select	ENSP00000496564.2:n.981-28C>T
ENST00000647277.1:c.980+4114C>T	ENSP00000495594.1:n.980+4114C>T
ENST00000286149.8:c.1023-28C>T	ENSP00000286149.4:n.1023-28C>T
ENST00000388956.8:c.744-28C>T	ENSP00000373608.4:n.744-28C>T
ENST00000388957.3:c.9-28C>T	ENSP00000373609.3:n.9-28C>T
ENST00000388958.7:c.981-28C>T	ENSP00000373610.3:n.981-28C>T
ENST00000563871.5:n.173C>T
ENST00000569064.1:n.175C>T
NM_001161683.1:c.744-28C>T	NP_001155155.1:n.744-28C>T
NM_144672.3:c.981-28C>T	NP_653273.3:n.981-28C>T
NM_170664.2:c.9-28C>T	NP_733764.1:n.9-28C>T
XM_011545747.1:c.981-28C>T	XP_011544049.1:n.981-28C>T
XM_011545748.1:c.-331C>T	XP_011544050.1:n.-331C>T
NM_144672.4:c.981-28C>T MANE Select	NP_653273.3:n.981-28C>T
XM_011545748.2:c.-331C>T	XP_011544050.2:n.-331C>T
XR_002957775.1:n.76-28C>T
NM_001161683.2:c.744-28C>T	NP_001155155.1:n.744-28C>T
NM_170664.3:c.9-28C>T	NP_733764.1:n.9-28C>T