Canonical Allele Identifier: CA2747716395
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640768_215640769del , CM000663.2:g.215640768_215640769del GRCh38
NC_000001.10:g.215814110_215814111del , CM000663.1:g.215814110_215814111del GRCh37
NC_000001.9:g.213880733_213880734del NCBI36
NG_009497.1:g.787628_787629del
NG_009497.2:g.787680_787681del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14792-35_14792-34del MANE Select ENSP00000305941.3:n.14792-35_14792-34del
ENST00000674083.1:c.14792-35_14792-34del ENSP00000501296.1:n.14792-35_14792-34del
ENST00000307340.7:c.14792-35_14792-34del ENSP00000305941.3:n.14792-35_14792-34del
NM_206933.2:c.14792-35_14792-34del NP_996816.2:n.14792-35_14792-34del
NM_206933.3:c.14792-35_14792-34del NP_996816.2:n.14792-35_14792-34del
NM_206933.4:c.14792-35_14792-34del MANE Select NP_996816.3:n.14792-35_14792-34del