Canonical Allele Identifier: CA2747719090
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728445_215728446insC , CM000663.2:g.215728445_215728446insC GRCh38
NC_000001.10:g.215901787_215901788insC , CM000663.1:g.215901787_215901788insC GRCh37
NC_000001.9:g.213968410_213968411insC NCBI36
NG_009497.1:g.699951_699952insG
NG_009497.2:g.700003_700004insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-62_11712-61insG MANE Select ENSP00000305941.3:n.11712-62_11712-61insG
ENST00000674083.1:c.11712-62_11712-61insG ENSP00000501296.1:n.11712-62_11712-61insG
ENST00000307340.7:c.11712-62_11712-61insG ENSP00000305941.3:n.11712-62_11712-61insG
NM_206933.2:c.11712-62_11712-61insG NP_996816.2:n.11712-62_11712-61insG
NM_206933.3:c.11712-62_11712-61insG NP_996816.2:n.11712-62_11712-61insG
NM_206933.4:c.11712-62_11712-61insG MANE Select NP_996816.3:n.11712-62_11712-61insG