Canonical Allele Identifier: CA2747719159
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728548_215728554del , CM000663.2:g.215728548_215728554del GRCh38
NC_000001.10:g.215901890_215901896del , CM000663.1:g.215901890_215901896del GRCh37
NC_000001.9:g.213968513_213968519del NCBI36
NG_009497.1:g.699843_699849del
NG_009497.2:g.699895_699901del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-170_11712-164del MANE Select ENSP00000305941.3:n.11712-170_11712-164del
ENST00000674083.1:c.11712-170_11712-164del ENSP00000501296.1:n.11712-170_11712-164del
ENST00000307340.7:c.11712-170_11712-164del ENSP00000305941.3:n.11712-170_11712-164del
NM_206933.2:c.11712-170_11712-164del NP_996816.2:n.11712-170_11712-164del
NM_206933.3:c.11712-170_11712-164del NP_996816.2:n.11712-170_11712-164del
NM_206933.4:c.11712-170_11712-164del MANE Select NP_996816.3:n.11712-170_11712-164del