Canonical Allele Identifier: CA2747720804
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780141_215780147del , CM000663.2:g.215780141_215780147del GRCh38
NC_000001.10:g.215953483_215953489del , CM000663.1:g.215953483_215953489del GRCh37
NC_000001.9:g.214020106_214020112del NCBI36
NG_009497.1:g.648250_648256del
NG_009497.2:g.648302_648308del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-106_10741-100del MANE Select ENSP00000305941.3:n.10741-106_10741-100del
ENST00000674083.1:c.10741-106_10741-100del ENSP00000501296.1:n.10741-106_10741-100del
ENST00000307340.7:c.10741-106_10741-100del ENSP00000305941.3:n.10741-106_10741-100del
NM_206933.2:c.10741-106_10741-100del NP_996816.2:n.10741-106_10741-100del
NM_206933.3:c.10741-106_10741-100del NP_996816.2:n.10741-106_10741-100del
NM_206933.4:c.10741-106_10741-100del MANE Select NP_996816.3:n.10741-106_10741-100del