Canonical Allele Identifier: CA2650499105
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640862_215640863insAAAAACAAACCAACCCCAAAAAAAAAAAAAAAAAAAAA , CM000663.2:g.215640862_215640863insAAAAACAAACCAACCCCAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000001.10:g.215814204_215814205insAAAAACAAACCAACCCCAAAAAAAAAAAAAAAAAAAAA , CM000663.1:g.215814204_215814205insAAAAACAAACCAACCCCAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000001.9:g.213880827_213880828insAAAAACAAACCAACCCCAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_009497.1:g.787552_787553insTTTGGGGTTGGTTTGTTTTTTTTTTTTTTTTTTTTTTT
NG_009497.2:g.787604_787605insTTTGGGGTTGGTTTGTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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