Canonical Allele Identifier: CA1396209
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs753670817

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216246829del , CM000663.2:g.216246829del GRCh38
NC_000001.10:g.216420171del , CM000663.1:g.216420171del GRCh37
NC_000001.9:g.214486794del NCBI36
NG_009497.1:g.181570del
NG_009497.2:g.181622del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2567del MANE Select ENSP00000305941.3:p.Asn856MetfsTer17
ENST00000674083.1:c.2567del ENSP00000501296.1:p.Asn856MetfsTer17
ENST00000307340.7:c.2567del ENSP00000305941.3:p.Asn856MetfsTer17
ENST00000366942.3:c.2567del ENSP00000355909.3:p.Asn856MetfsTer17
NM_007123.5:c.2567del NP_009054.5:p.Asn856MetfsTer17
NM_206933.2:c.2567del NP_996816.2:p.Asn856MetfsTer17
NM_206933.3:c.2567del NP_996816.2:p.Asn856MetfsTer17
NM_007123.6:c.2567del NP_009054.6:p.Asn856MetfsTer17
NM_206933.4:c.2567del MANE Select NP_996816.3:p.Asn856MetfsTer17