Canonical Allele Identifier: CA2747722522
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215817259_215817260del , CM000663.2:g.215817259_215817260del GRCh38
NC_000001.10:g.215990601_215990602del , CM000663.1:g.215990601_215990602del GRCh37
NC_000001.9:g.214057224_214057225del NCBI36
NG_009497.1:g.611137_611138del
NG_009497.2:g.611189_611190del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9372-65_9372-64del MANE Select ENSP00000305941.3:n.9372-65_9372-64del
ENST00000674083.1:c.9372-65_9372-64del ENSP00000501296.1:n.9372-65_9372-64del
ENST00000307340.7:c.9372-65_9372-64del ENSP00000305941.3:n.9372-65_9372-64del
NM_206933.2:c.9372-65_9372-64del NP_996816.2:n.9372-65_9372-64del
NM_206933.3:c.9372-65_9372-64del NP_996816.2:n.9372-65_9372-64del
NM_206933.4:c.9372-65_9372-64del MANE Select NP_996816.3:n.9372-65_9372-64del