Canonical Allele Identifier: CA2747729431
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216070426_216070427insAG , CM000663.2:g.216070426_216070427insAG GRCh38
NC_000001.10:g.216243768_216243769insAG , CM000663.1:g.216243768_216243769insAG GRCh37
NC_000001.9:g.214310391_214310392insAG NCBI36
NG_009497.1:g.357970_357971insCT
NG_009497.2:g.358022_358023insCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.5858-135_5858-134insCT MANE Select ENSP00000305941.3:n.5858-135_5858-134insCT
ENST00000674083.1:c.5858-135_5858-134insCT ENSP00000501296.1:n.5858-135_5858-134insCT
ENST00000307340.7:c.5858-135_5858-134insCT ENSP00000305941.3:n.5858-135_5858-134insCT
NM_206933.2:c.5858-135_5858-134insCT NP_996816.2:n.5858-135_5858-134insCT
NM_206933.3:c.5858-135_5858-134insCT NP_996816.2:n.5858-135_5858-134insCT
NM_206933.4:c.5858-135_5858-134insCT MANE Select NP_996816.3:n.5858-135_5858-134insCT