Canonical Allele Identifier: CA2747720814
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780145_215780146insAGT , CM000663.2:g.215780145_215780146insAGT GRCh38
NC_000001.10:g.215953487_215953488insAGT , CM000663.1:g.215953487_215953488insAGT GRCh37
NC_000001.9:g.214020110_214020111insAGT NCBI36
NG_009497.1:g.648251_648252insACT
NG_009497.2:g.648303_648304insACT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-105_10741-104insACT MANE Select ENSP00000305941.3:n.10741-105_10741-104insACT
ENST00000674083.1:c.10741-105_10741-104insACT ENSP00000501296.1:n.10741-105_10741-104insACT
ENST00000307340.7:c.10741-105_10741-104insACT ENSP00000305941.3:n.10741-105_10741-104insACT
NM_206933.2:c.10741-105_10741-104insACT NP_996816.2:n.10741-105_10741-104insACT
NM_206933.3:c.10741-105_10741-104insACT NP_996816.2:n.10741-105_10741-104insACT
NM_206933.4:c.10741-105_10741-104insACT MANE Select NP_996816.3:n.10741-105_10741-104insACT