Canonical Allele Identifier: CA10581501
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 236049
ClinVar RCV Id: RCV000225050
dbSNP Id: rs878853233

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215813791del , CM000663.2:g.215813791del GRCh38
NC_000001.10:g.215987133del , CM000663.1:g.215987133del GRCh37
NC_000001.9:g.214053756del NCBI36
NG_009497.1:g.614607del
NG_009497.2:g.614659del

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.9685del MANE Select ENSP00000305941.3:p.Glu3229ArgfsTer?
ENST00000674083.1:c.9685del ENSP00000501296.1:p.Glu3229ArgfsTer?
ENST00000307340.7:c.9685del ENSP00000305941.3:p.Glu3229ArgfsTer?
NM_206933.2:c.9685del NP_996816.2:p.Glu3229ArgfsTer?
NM_206933.3:c.9685del NP_996816.2:p.Glu3229ArgfsTer?
NM_206933.4:c.9685del MANE Select NP_996816.3:p.Glu3229ArgfsTer?