Canonical Allele Identifier: CA1220396649
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728548_215728549delinsTG , CM000663.2:g.215728548_215728549delinsTG GRCh38
NC_000001.10:g.215901890_215901891delinsTG , CM000663.1:g.215901890_215901891delinsTG GRCh37
NC_000001.9:g.213968513_213968514delinsTG NCBI36
NG_009497.1:g.699848_699849delinsCA
NG_009497.2:g.699900_699901delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-165_11712-164delinsCA MANE Select ENSP00000305941.3:n.11712-165_11712-164delinsCA
ENST00000674083.1:c.11712-165_11712-164delinsCA ENSP00000501296.1:n.11712-165_11712-164delinsCA
ENST00000307340.7:c.11712-165_11712-164delinsCA ENSP00000305941.3:n.11712-165_11712-164delinsCA
NM_206933.2:c.11712-165_11712-164delinsCA NP_996816.2:n.11712-165_11712-164delinsCA
NM_206933.3:c.11712-165_11712-164delinsCA NP_996816.2:n.11712-165_11712-164delinsCA
NM_206933.4:c.11712-165_11712-164delinsCA MANE Select NP_996816.3:n.11712-165_11712-164delinsCA