Canonical Allele Identifier: CA1012179146
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2702672
ClinVar RCV Id: RCV003577483
dbSNP Id: rs1657981723

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675270del , CM000663.2:g.215675270del GRCh38
NC_000001.10:g.215848612del , CM000663.1:g.215848612del GRCh37
NC_000001.9:g.213915235del NCBI36
NG_009497.1:g.753127del
NG_009497.2:g.753179del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12641del MANE Select ENSP00000305941.3:p.Thr4214LysfsTer?
ENST00000674083.1:c.12641del ENSP00000501296.1:p.Thr4214LysfsTer?
ENST00000307340.7:c.12641del ENSP00000305941.3:p.Thr4214LysfsTer?
NM_206933.2:c.12641del NP_996816.2:p.Thr4214LysfsTer?
NM_206933.3:c.12641del NP_996816.2:p.Thr4214LysfsTer?
NM_206933.4:c.12641del MANE Select NP_996816.3:p.Thr4214LysfsTer?