Canonical Allele Identifier: CA2747722582
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215817296_215817301del , CM000663.2:g.215817296_215817301del GRCh38
NC_000001.10:g.215990638_215990643del , CM000663.1:g.215990638_215990643del GRCh37
NC_000001.9:g.214057261_214057266del NCBI36
NG_009497.1:g.611103_611108del
NG_009497.2:g.611155_611160del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9372-99_9372-94del MANE Select ENSP00000305941.3:n.9372-99_9372-94del
ENST00000674083.1:c.9372-99_9372-94del ENSP00000501296.1:n.9372-99_9372-94del
ENST00000307340.7:c.9372-99_9372-94del ENSP00000305941.3:n.9372-99_9372-94del
NM_206933.2:c.9372-99_9372-94del NP_996816.2:n.9372-99_9372-94del
NM_206933.3:c.9372-99_9372-94del NP_996816.2:n.9372-99_9372-94del
NM_206933.4:c.9372-99_9372-94del MANE Select NP_996816.3:n.9372-99_9372-94del