Canonical Allele Identifier: CA2747720848
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780160_215780163del , CM000663.2:g.215780160_215780163del GRCh38
NC_000001.10:g.215953502_215953505del , CM000663.1:g.215953502_215953505del GRCh37
NC_000001.9:g.214020125_214020128del NCBI36
NG_009497.1:g.648234_648237del
NG_009497.2:g.648286_648289del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-122_10741-119del MANE Select ENSP00000305941.3:n.10741-122_10741-119del
ENST00000674083.1:c.10741-122_10741-119del ENSP00000501296.1:n.10741-122_10741-119del
ENST00000307340.7:c.10741-122_10741-119del ENSP00000305941.3:n.10741-122_10741-119del
NM_206933.2:c.10741-122_10741-119del NP_996816.2:n.10741-122_10741-119del
NM_206933.3:c.10741-122_10741-119del NP_996816.2:n.10741-122_10741-119del
NM_206933.4:c.10741-122_10741-119del MANE Select NP_996816.3:n.10741-122_10741-119del