Canonical Allele Identifier: CA1220619249
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247094_216247095delinsTC , CM000663.2:g.216247094_216247095delinsTC GRCh38
NC_000001.10:g.216420436_216420437delinsTC , CM000663.1:g.216420436_216420437delinsTC GRCh37
NC_000001.9:g.214487059_214487060delinsTC NCBI36
NG_009497.1:g.181302_181303delinsGA
NG_009497.2:g.181354_181355delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2299_2300delinsGA MANE Select ENSP00000305941.3:p.Glu767=
ENST00000674083.1:c.2299_2300delinsGA ENSP00000501296.1:p.Glu767=
ENST00000307340.7:c.2299_2300delinsGA ENSP00000305941.3:p.Glu767=
ENST00000366942.3:c.2299_2300delinsGA ENSP00000355909.3:p.Glu767=
NM_007123.5:c.2299_2300delinsGA NP_009054.5:p.Glu767=
NM_206933.2:c.2299_2300delinsGA NP_996816.2:p.Glu767=
NM_206933.3:c.2299_2300delinsGA NP_996816.2:p.Glu767=
NM_007123.6:c.2299_2300delinsGA NP_009054.6:p.Glu767=
NM_206933.4:c.2299_2300delinsGA MANE Select NP_996816.3:p.Glu767=