Canonical Allele Identifier: CA1220619062
Gene: USH2A HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216246632_216246633delinsAG , CM000663.2:g.216246632_216246633delinsAG GRCh38
NC_000001.10:g.216419974_216419975delinsAG , CM000663.1:g.216419974_216419975delinsAG GRCh37
NC_000001.9:g.214486597_214486598delinsAG NCBI36
NG_009497.1:g.181764_181765delinsCT
NG_009497.2:g.181816_181817delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2761_2762delinsCT MANE Select ENSP00000305941.3:p.Leu921=
ENST00000674083.1:c.2761_2762delinsCT ENSP00000501296.1:p.Leu921=
ENST00000307340.7:c.2761_2762delinsCT ENSP00000305941.3:p.Leu921=
ENST00000366942.3:c.2761_2762delinsCT ENSP00000355909.3:p.Leu921=
NM_007123.5:c.2761_2762delinsCT NP_009054.5:p.Leu921=
NM_206933.2:c.2761_2762delinsCT NP_996816.2:p.Leu921=
NM_206933.3:c.2761_2762delinsCT NP_996816.2:p.Leu921=
NM_007123.6:c.2761_2762delinsCT NP_009054.6:p.Leu921=
NM_206933.4:c.2761_2762delinsCT MANE Select NP_996816.3:p.Leu921=
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