Canonical Allele Identifier: CA2747719109
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728462_215728463insACA , CM000663.2:g.215728462_215728463insACA GRCh38
NC_000001.10:g.215901804_215901805insACA , CM000663.1:g.215901804_215901805insACA GRCh37
NC_000001.9:g.213968427_213968428insACA NCBI36
NG_009497.1:g.699934_699935insTGT
NG_009497.2:g.699986_699987insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-79_11712-78insTGT MANE Select ENSP00000305941.3:n.11712-79_11712-78insTGT
ENST00000674083.1:c.11712-79_11712-78insTGT ENSP00000501296.1:n.11712-79_11712-78insTGT
ENST00000307340.7:c.11712-79_11712-78insTGT ENSP00000305941.3:n.11712-79_11712-78insTGT
NM_206933.2:c.11712-79_11712-78insTGT NP_996816.2:n.11712-79_11712-78insTGT
NM_206933.3:c.11712-79_11712-78insTGT NP_996816.2:n.11712-79_11712-78insTGT
NM_206933.4:c.11712-79_11712-78insTGT MANE Select NP_996816.3:n.11712-79_11712-78insTGT