Canonical Allele Identifier: CA2650504877
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867228_215867229del , CM000663.2:g.215867228_215867229del GRCh38
NC_000001.10:g.216040570_216040571del , CM000663.1:g.216040570_216040571del GRCh37
NC_000001.9:g.214107193_214107194del NCBI36
NG_009497.1:g.561169_561170del
NG_009497.2:g.561221_561222del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8682-58_8682-57del MANE Select ENSP00000305941.3:n.8682-58_8682-57del
ENST00000674083.1:c.8682-58_8682-57del ENSP00000501296.1:n.8682-58_8682-57del
ENST00000307340.7:c.8682-58_8682-57del ENSP00000305941.3:n.8682-58_8682-57del
NM_206933.2:c.8682-58_8682-57del NP_996816.2:n.8682-58_8682-57del
NM_206933.3:c.8682-58_8682-57del NP_996816.2:n.8682-58_8682-57del
NM_206933.4:c.8682-58_8682-57del MANE Select NP_996816.3:n.8682-58_8682-57del