Canonical Allele Identifier: CA2747719096
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728447_215728448insA , CM000663.2:g.215728447_215728448insA GRCh38
NC_000001.10:g.215901789_215901790insA , CM000663.1:g.215901789_215901790insA GRCh37
NC_000001.9:g.213968412_213968413insA NCBI36
NG_009497.1:g.699949_699950insT
NG_009497.2:g.700001_700002insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-64_11712-63insT MANE Select ENSP00000305941.3:n.11712-64_11712-63insT
ENST00000674083.1:c.11712-64_11712-63insT ENSP00000501296.1:n.11712-64_11712-63insT
ENST00000307340.7:c.11712-64_11712-63insT ENSP00000305941.3:n.11712-64_11712-63insT
NM_206933.2:c.11712-64_11712-63insT NP_996816.2:n.11712-64_11712-63insT
NM_206933.3:c.11712-64_11712-63insT NP_996816.2:n.11712-64_11712-63insT
NM_206933.4:c.11712-64_11712-63insT MANE Select NP_996816.3:n.11712-64_11712-63insT