Canonical Allele Identifier: CA2747719082
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728438_215728448del , CM000663.2:g.215728438_215728448del GRCh38
NC_000001.10:g.215901780_215901790del , CM000663.1:g.215901780_215901790del GRCh37
NC_000001.9:g.213968403_213968413del NCBI36
NG_009497.1:g.699950_699960del
NG_009497.2:g.700002_700012del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-63_11712-53del MANE Select ENSP00000305941.3:n.11712-63_11712-53del
ENST00000674083.1:c.11712-63_11712-53del ENSP00000501296.1:n.11712-63_11712-53del
ENST00000307340.7:c.11712-63_11712-53del ENSP00000305941.3:n.11712-63_11712-53del
NM_206933.2:c.11712-63_11712-53del NP_996816.2:n.11712-63_11712-53del
NM_206933.3:c.11712-63_11712-53del NP_996816.2:n.11712-63_11712-53del
NM_206933.4:c.11712-63_11712-53del MANE Select NP_996816.3:n.11712-63_11712-53del