Canonical Allele Identifier: CA2747720805
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780142del , CM000663.2:g.215780142del GRCh38
NC_000001.10:g.215953484del , CM000663.1:g.215953484del GRCh37
NC_000001.9:g.214020107del NCBI36
NG_009497.1:g.648255del
NG_009497.2:g.648307del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-101del MANE Select ENSP00000305941.3:n.10741-101del
ENST00000674083.1:c.10741-101del ENSP00000501296.1:n.10741-101del
ENST00000307340.7:c.10741-101del ENSP00000305941.3:n.10741-101del
NM_206933.2:c.10741-101del NP_996816.2:n.10741-101del
NM_206933.3:c.10741-101del NP_996816.2:n.10741-101del
NM_206933.4:c.10741-101del MANE Select NP_996816.3:n.10741-101del