Canonical Allele Identifier: CA1220373872
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675269_215675270delinsTG , CM000663.2:g.215675269_215675270delinsTG GRCh38
NC_000001.10:g.215848611_215848612delinsTG , CM000663.1:g.215848611_215848612delinsTG GRCh37
NC_000001.9:g.213915234_213915235delinsTG NCBI36
NG_009497.1:g.753127_753128delinsCA
NG_009497.2:g.753179_753180delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12641_12642delinsCA MANE Select ENSP00000305941.3:p.Thr4214=
ENST00000674083.1:c.12641_12642delinsCA ENSP00000501296.1:p.Thr4214=
ENST00000307340.7:c.12641_12642delinsCA ENSP00000305941.3:p.Thr4214=
NM_206933.2:c.12641_12642delinsCA NP_996816.2:p.Thr4214=
NM_206933.3:c.12641_12642delinsCA NP_996816.2:p.Thr4214=
NM_206933.4:c.12641_12642delinsCA MANE Select NP_996816.3:p.Thr4214=