Canonical Allele Identifier: CA395062264

Gene: OTOA

Linked Data

• MyVariant Identifiers: chr16:g.21721279A>T (hg19) ; chr16:g.21709958A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21709958A>T , CM000678.2:g.21709958A>T	GRCh38
NC_000016.9:g.21721279A>T , CM000678.1:g.21721279A>T	GRCh37
NC_000016.8:g.21628780A>T	NCBI36
NG_012973.1:g.36445A>T
NG_012973.2:g.50826A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1175A>T	ENSP00000373610.3:p.Asp392Val
ENST00000646100.2:c.1175A>T MANE Select	ENSP00000496564.2:p.Asp392Val
ENST00000647277.1:c.1051A>T	ENSP00000495594.1:p.Met351Leu
ENST00000286149.8:c.1217A>T	ENSP00000286149.4:p.Asp406Val
ENST00000388956.8:c.938A>T	ENSP00000373608.4:p.Asp313Val
ENST00000388957.3:c.203A>T	ENSP00000373609.3:p.Asp68Val
ENST00000388958.7:c.1175A>T	ENSP00000373610.3:p.Asp392Val
ENST00000563871.5:n.395A>T
NM_001161683.1:c.938A>T	NP_001155155.1:p.Asp313Val
NM_144672.3:c.1175A>T	NP_653273.3:p.Asp392Val
NM_170664.2:c.203A>T	NP_733764.1:p.Asp68Val
XM_011545747.1:c.1175A>T	XP_011544049.1:p.Asp392Val
XM_011545748.1:c.44A>T	XP_011544050.1:p.Asp15Val
NM_144672.4:c.1175A>T MANE Select	NP_653273.3:p.Asp392Val
XM_011545748.2:c.44A>T	XP_011544050.2:p.Asp15Val
XR_002957775.1:n.270A>T
NM_001161683.2:c.938A>T	NP_001155155.1:p.Asp313Val
NM_170664.3:c.203A>T	NP_733764.1:p.Asp68Val