Canonical Allele Identifier: CA2747716502
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640830_215640831insACA , CM000663.2:g.215640830_215640831insACA GRCh38
NC_000001.10:g.215814172_215814173insACA , CM000663.1:g.215814172_215814173insACA GRCh37
NC_000001.9:g.213880795_213880796insACA NCBI36
NG_009497.1:g.787566_787567insTGT
NG_009497.2:g.787618_787619insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14792-97_14792-96insTGT MANE Select ENSP00000305941.3:n.14792-97_14792-96insTGT
ENST00000674083.1:c.14792-97_14792-96insTGT ENSP00000501296.1:n.14792-97_14792-96insTGT
ENST00000307340.7:c.14792-97_14792-96insTGT ENSP00000305941.3:n.14792-97_14792-96insTGT
NM_206933.2:c.14792-97_14792-96insTGT NP_996816.2:n.14792-97_14792-96insTGT
NM_206933.3:c.14792-97_14792-96insTGT NP_996816.2:n.14792-97_14792-96insTGT
NM_206933.4:c.14792-97_14792-96insTGT MANE Select NP_996816.3:n.14792-97_14792-96insTGT