Canonical Allele Identifier: CA2747721877
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215799170_215799182del , CM000663.2:g.215799170_215799182del GRCh38
NC_000001.10:g.215972512_215972524del , CM000663.1:g.215972512_215972524del GRCh37
NC_000001.9:g.214039135_214039147del NCBI36
NG_009497.1:g.629216_629228del
NG_009497.2:g.629268_629280del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9740-56_9740-44del MANE Select ENSP00000305941.3:n.9740-56_9740-44del
ENST00000674083.1:c.9740-56_9740-44del ENSP00000501296.1:n.9740-56_9740-44del
ENST00000307340.7:c.9740-56_9740-44del ENSP00000305941.3:n.9740-56_9740-44del
NM_206933.2:c.9740-56_9740-44del NP_996816.2:n.9740-56_9740-44del
NM_206933.3:c.9740-56_9740-44del NP_996816.2:n.9740-56_9740-44del
NM_206933.4:c.9740-56_9740-44del MANE Select NP_996816.3:n.9740-56_9740-44del