Canonical Allele Identifier: CA2747717703
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675660_215675661insAC , CM000663.2:g.215675660_215675661insAC GRCh38
NC_000001.10:g.215849002_215849003insAC , CM000663.1:g.215849002_215849003insAC GRCh37
NC_000001.9:g.213915625_213915626insAC NCBI36
NG_009497.1:g.752736_752737insGT
NG_009497.2:g.752788_752789insGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-45_12295-44insGT MANE Select ENSP00000305941.3:n.12295-45_12295-44insGT
ENST00000674083.1:c.12295-45_12295-44insGT ENSP00000501296.1:n.12295-45_12295-44insGT
ENST00000307340.7:c.12295-45_12295-44insGT ENSP00000305941.3:n.12295-45_12295-44insGT
NM_206933.2:c.12295-45_12295-44insGT NP_996816.2:n.12295-45_12295-44insGT
NM_206933.3:c.12295-45_12295-44insGT NP_996816.2:n.12295-45_12295-44insGT
NM_206933.4:c.12295-45_12295-44insGT MANE Select NP_996816.3:n.12295-45_12295-44insGT