Canonical Allele Identifier: CA2650499151
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640845_215640846insCAA , CM000663.2:g.215640845_215640846insCAA GRCh38
NC_000001.10:g.215814187_215814188insCAA , CM000663.1:g.215814187_215814188insCAA GRCh37
NC_000001.9:g.213880810_213880811insCAA NCBI36
NG_009497.1:g.787552_787553insTGT
NG_009497.2:g.787604_787605insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14792-111_14792-110insTGT MANE Select ENSP00000305941.3:n.14792-111_14792-110insTGT
ENST00000674083.1:c.14792-111_14792-110insTGT ENSP00000501296.1:n.14792-111_14792-110insTGT
ENST00000307340.7:c.14792-111_14792-110insTGT ENSP00000305941.3:n.14792-111_14792-110insTGT
NM_206933.2:c.14792-111_14792-110insTGT NP_996816.2:n.14792-111_14792-110insTGT
NM_206933.3:c.14792-111_14792-110insTGT NP_996816.2:n.14792-111_14792-110insTGT
NM_206933.4:c.14792-111_14792-110insTGT MANE Select NP_996816.3:n.14792-111_14792-110insTGT