Canonical Allele Identifier: CA2747720778
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780133_215780134insAC , CM000663.2:g.215780133_215780134insAC GRCh38
NC_000001.10:g.215953475_215953476insAC , CM000663.1:g.215953475_215953476insAC GRCh37
NC_000001.9:g.214020098_214020099insAC NCBI36
NG_009497.1:g.648264_648265insTG
NG_009497.2:g.648316_648317insTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-92_10741-91insTG MANE Select ENSP00000305941.3:n.10741-92_10741-91insTG
ENST00000674083.1:c.10741-92_10741-91insTG ENSP00000501296.1:n.10741-92_10741-91insTG
ENST00000307340.7:c.10741-92_10741-91insTG ENSP00000305941.3:n.10741-92_10741-91insTG
NM_206933.2:c.10741-92_10741-91insTG NP_996816.2:n.10741-92_10741-91insTG
NM_206933.3:c.10741-92_10741-91insTG NP_996816.2:n.10741-92_10741-91insTG
NM_206933.4:c.10741-92_10741-91insTG MANE Select NP_996816.3:n.10741-92_10741-91insTG