Canonical Allele Identifier: CA2747720858
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780165_215780168del , CM000663.2:g.215780165_215780168del GRCh38
NC_000001.10:g.215953507_215953510del , CM000663.1:g.215953507_215953510del GRCh37
NC_000001.9:g.214020130_214020133del NCBI36
NG_009497.1:g.648229_648232del
NG_009497.2:g.648281_648284del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-127_10741-124del MANE Select ENSP00000305941.3:n.10741-127_10741-124del
ENST00000674083.1:c.10741-127_10741-124del ENSP00000501296.1:n.10741-127_10741-124del
ENST00000307340.7:c.10741-127_10741-124del ENSP00000305941.3:n.10741-127_10741-124del
NM_206933.2:c.10741-127_10741-124del NP_996816.2:n.10741-127_10741-124del
NM_206933.3:c.10741-127_10741-124del NP_996816.2:n.10741-127_10741-124del
NM_206933.4:c.10741-127_10741-124del MANE Select NP_996816.3:n.10741-127_10741-124del