Canonical Allele Identifier: CA2747720887
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780174_215780175insACA , CM000663.2:g.215780174_215780175insACA GRCh38
NC_000001.10:g.215953516_215953517insACA , CM000663.1:g.215953516_215953517insACA GRCh37
NC_000001.9:g.214020139_214020140insACA NCBI36
NG_009497.1:g.648222_648223insTGT
NG_009497.2:g.648274_648275insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-134_10741-133insTGT MANE Select ENSP00000305941.3:n.10741-134_10741-133insTGT
ENST00000674083.1:c.10741-134_10741-133insTGT ENSP00000501296.1:n.10741-134_10741-133insTGT
ENST00000307340.7:c.10741-134_10741-133insTGT ENSP00000305941.3:n.10741-134_10741-133insTGT
NM_206933.2:c.10741-134_10741-133insTGT NP_996816.2:n.10741-134_10741-133insTGT
NM_206933.3:c.10741-134_10741-133insTGT NP_996816.2:n.10741-134_10741-133insTGT
NM_206933.4:c.10741-134_10741-133insTGT MANE Select NP_996816.3:n.10741-134_10741-133insTGT