Canonical Allele Identifier: CA2499214518
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1072288
ClinVar RCV Id: RCV001384972
dbSNP Id: rs2102546166

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247091del , CM000663.2:g.216247091del GRCh38
NC_000001.10:g.216420433del , CM000663.1:g.216420433del GRCh37
NC_000001.9:g.214487056del NCBI36
NG_009497.1:g.181306del
NG_009497.2:g.181358del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2303del MANE Select ENSP00000305941.3:p.Cys768SerfsTer20
ENST00000674083.1:c.2303del ENSP00000501296.1:p.Cys768SerfsTer20
ENST00000307340.7:c.2303del ENSP00000305941.3:p.Cys768SerfsTer20
ENST00000366942.3:c.2303del ENSP00000355909.3:p.Cys768SerfsTer20
NM_007123.5:c.2303del NP_009054.5:p.Cys768SerfsTer20
NM_206933.2:c.2303del NP_996816.2:p.Cys768SerfsTer20
NM_206933.3:c.2303del NP_996816.2:p.Cys768SerfsTer20
NM_007123.6:c.2303del NP_009054.6:p.Cys768SerfsTer20
NM_206933.4:c.2303del MANE Select NP_996816.3:p.Cys768SerfsTer20