Canonical Allele Identifier: CA2747719163
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728561_215728563del , CM000663.2:g.215728561_215728563del GRCh38
NC_000001.10:g.215901903_215901905del , CM000663.1:g.215901903_215901905del GRCh37
NC_000001.9:g.213968526_213968528del NCBI36
NG_009497.1:g.699834_699836del
NG_009497.2:g.699886_699888del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-179_11712-177del MANE Select ENSP00000305941.3:n.11712-179_11712-177del
ENST00000674083.1:c.11712-179_11712-177del ENSP00000501296.1:n.11712-179_11712-177del
ENST00000307340.7:c.11712-179_11712-177del ENSP00000305941.3:n.11712-179_11712-177del
NM_206933.2:c.11712-179_11712-177del NP_996816.2:n.11712-179_11712-177del
NM_206933.3:c.11712-179_11712-177del NP_996816.2:n.11712-179_11712-177del
NM_206933.4:c.11712-179_11712-177del MANE Select NP_996816.3:n.11712-179_11712-177del