Canonical Allele Identifier: CA2581255667

Gene: OTOA

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21709871G>C , CM000678.2:g.21709871G>C	GRCh38
NC_000016.9:g.21721192G>C , CM000678.1:g.21721192G>C	GRCh37
NC_000016.8:g.21628693G>C	NCBI36
NG_012973.1:g.36358G>C
NG_012973.2:g.50739G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000388958.8:c.1105-17G>C	ENSP00000373610.3:n.1105-17G>C
ENST00000646100.2:c.1105-17G>C MANE Select	ENSP00000496564.2:n.1105-17G>C
ENST00000647277.1:c.981-17G>C	ENSP00000495594.1:n.981-17G>C
ENST00000286149.8:c.1147-17G>C	ENSP00000286149.4:n.1147-17G>C
ENST00000388956.8:c.868-17G>C	ENSP00000373608.4:n.868-17G>C
ENST00000388957.3:c.133-17G>C	ENSP00000373609.3:n.133-17G>C
ENST00000388958.7:c.1105-17G>C	ENSP00000373610.3:n.1105-17G>C
ENST00000563871.5:n.325-17G>C
ENST00000569064.1:n.479-17G>C
NM_001161683.1:c.868-17G>C	NP_001155155.1:n.868-17G>C
NM_144672.3:c.1105-17G>C	NP_653273.3:n.1105-17G>C
NM_170664.2:c.133-17G>C	NP_733764.1:n.133-17G>C
XM_011545747.1:c.1105-17G>C	XP_011544049.1:n.1105-17G>C
XM_011545748.1:c.-27-17G>C	XP_011544050.1:n.-27-17G>C
NM_144672.4:c.1105-17G>C MANE Select	NP_653273.3:n.1105-17G>C
XM_011545748.2:c.-27-17G>C	XP_011544050.2:n.-27-17G>C
XR_002957775.1:n.200-17G>C
NM_001161683.2:c.868-17G>C	NP_001155155.1:n.868-17G>C
NM_170664.3:c.133-17G>C	NP_733764.1:n.133-17G>C