Canonical Allele Identifier: CA494111073

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21739603G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21728282G>C , CM000678.2:g.21728282G>C	GRCh38
NC_000016.9:g.21739603G>C , CM000678.1:g.21739603G>C	GRCh37
NC_000016.8:g.21647104G>C	NCBI36
NG_012973.1:g.54769G>C
NG_012973.2:g.69150G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000388958.8:c.2058G>C	ENSP00000373610.3:p.Gly686=
ENST00000646100.2:c.2058G>C MANE Select	ENSP00000496564.2:p.Gly686=
ENST00000647277.1:c.*872G>C	ENSP00000495594.1:n.*872G>C
ENST00000286149.8:c.2100G>C	ENSP00000286149.4:p.Gly700=
ENST00000388956.8:c.1821G>C	ENSP00000373608.4:p.Gly607=
ENST00000388957.3:c.1086G>C	ENSP00000373609.3:p.Gly362=
ENST00000388958.7:c.2058G>C	ENSP00000373610.3:p.Gly686=
ENST00000563871.5:n.1521G>C
NM_001161683.1:c.1821G>C	NP_001155155.1:p.Gly607=
NM_144672.3:c.2058G>C	NP_653273.3:p.Gly686=
NM_170664.2:c.1086G>C	NP_733764.1:p.Gly362=
XM_011545747.1:c.2058G>C	XP_011544049.1:p.Gly686=
XM_011545748.1:c.927G>C	XP_011544050.1:p.Gly309=
NM_144672.4:c.2058G>C MANE Select	NP_653273.3:p.Gly686=
XM_011545748.2:c.927G>C	XP_011544050.2:p.Gly309=
XM_017022951.1:c.324G>C	XP_016878440.1:p.Gly108=
XR_002957775.1:n.1153G>C
NM_001161683.2:c.1821G>C	NP_001155155.1:p.Gly607=
NM_170664.3:c.1086G>C	NP_733764.1:p.Gly362=