Canonical Allele Identifier: CA37395809
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1054570220

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728666_215728668del , CM000663.2:g.215728666_215728668del GRCh38
NC_000001.10:g.215902008_215902010del , CM000663.1:g.215902008_215902010del GRCh37
NC_000001.9:g.213968631_213968633del NCBI36
NG_009497.1:g.699733_699735del
NG_009497.2:g.699785_699787del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-280_11712-278del MANE Select ENSP00000305941.3:n.11712-280_11712-278del
ENST00000674083.1:c.11712-280_11712-278del ENSP00000501296.1:n.11712-280_11712-278del
ENST00000307340.7:c.11712-280_11712-278del ENSP00000305941.3:n.11712-280_11712-278del
NM_206933.2:c.11712-280_11712-278del NP_996816.2:n.11712-280_11712-278del
NM_206933.3:c.11712-280_11712-278del NP_996816.2:n.11712-280_11712-278del
NM_206933.4:c.11712-280_11712-278del MANE Select NP_996816.3:n.11712-280_11712-278del