Canonical Allele Identifier: CA2747724432
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867300_215867301insA , CM000663.2:g.215867300_215867301insA GRCh38
NC_000001.10:g.216040642_216040643insA , CM000663.1:g.216040642_216040643insA GRCh37
NC_000001.9:g.214107265_214107266insA NCBI36
NG_009497.1:g.561096_561097insT
NG_009497.2:g.561148_561149insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8682-131_8682-130insT MANE Select ENSP00000305941.3:n.8682-131_8682-130insT
ENST00000674083.1:c.8682-131_8682-130insT ENSP00000501296.1:n.8682-131_8682-130insT
ENST00000307340.7:c.8682-131_8682-130insT ENSP00000305941.3:n.8682-131_8682-130insT
NM_206933.2:c.8682-131_8682-130insT NP_996816.2:n.8682-131_8682-130insT
NM_206933.3:c.8682-131_8682-130insT NP_996816.2:n.8682-131_8682-130insT
NM_206933.4:c.8682-131_8682-130insT MANE Select NP_996816.3:n.8682-131_8682-130insT