Canonical Allele Identifier: CA279402758

Gene: OTOA

Linked Data

• dbSNP Id: rs902897802
• MyVariant Identifiers: chr16:g.21716537C>G (hg19) ; chr16:g.21705216C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.21705216C>G , CM000678.2:g.21705216C>G	GRCh38
NC_000016.9:g.21716537C>G , CM000678.1:g.21716537C>G	GRCh37
NC_000016.8:g.21624038C>G	NCBI36
NG_012973.1:g.31703C>G
NG_012973.2:g.46084C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000388958.8:c.1028C>G	ENSP00000373610.3:p.Ala343Gly
ENST00000646100.2:c.1028C>G MANE Select	ENSP00000496564.2:p.Ala343Gly
ENST00000647277.1:c.980+4189C>G	ENSP00000495594.1:n.980+4189C>G
ENST00000286149.8:c.1070C>G	ENSP00000286149.4:p.Ala357Gly
ENST00000388956.8:c.791C>G	ENSP00000373608.4:p.Ala264Gly
ENST00000388957.3:c.56C>G	ENSP00000373609.3:p.Ala19Gly
ENST00000388958.7:c.1028C>G	ENSP00000373610.3:p.Ala343Gly
ENST00000563871.5:n.248C>G
ENST00000569064.1:n.250C>G
NM_001161683.1:c.791C>G	NP_001155155.1:p.Ala264Gly
NM_144672.3:c.1028C>G	NP_653273.3:p.Ala343Gly
NM_170664.2:c.56C>G	NP_733764.1:p.Ala19Gly
XM_011545747.1:c.1028C>G	XP_011544049.1:p.Ala343Gly
XM_011545748.1:c.-256C>G	XP_011544050.1:n.-256C>G
NM_144672.4:c.1028C>G MANE Select	NP_653273.3:p.Ala343Gly
XM_011545748.2:c.-256C>G	XP_011544050.2:n.-256C>G
XR_002957775.1:n.123C>G
NM_001161683.2:c.791C>G	NP_001155155.1:p.Ala264Gly
NM_170664.3:c.56C>G	NP_733764.1:p.Ala19Gly