Canonical Allele Identifier: CA2747722518
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215817257_215817261del , CM000663.2:g.215817257_215817261del GRCh38
NC_000001.10:g.215990599_215990603del , CM000663.1:g.215990599_215990603del GRCh37
NC_000001.9:g.214057222_214057226del NCBI36
NG_009497.1:g.611136_611140del
NG_009497.2:g.611188_611192del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9372-66_9372-62del MANE Select ENSP00000305941.3:n.9372-66_9372-62del
ENST00000674083.1:c.9372-66_9372-62del ENSP00000501296.1:n.9372-66_9372-62del
ENST00000307340.7:c.9372-66_9372-62del ENSP00000305941.3:n.9372-66_9372-62del
NM_206933.2:c.9372-66_9372-62del NP_996816.2:n.9372-66_9372-62del
NM_206933.3:c.9372-66_9372-62del NP_996816.2:n.9372-66_9372-62del
NM_206933.4:c.9372-66_9372-62del MANE Select NP_996816.3:n.9372-66_9372-62del