Canonical Allele Identifier: CA2747716525
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640862_215640863insAAAACCAACCCAACCCAAAAAAAAAAAAAAAAAAAAA , CM000663.2:g.215640862_215640863insAAAACCAACCCAACCCAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000001.10:g.215814204_215814205insAAAACCAACCCAACCCAAAAAAAAAAAAAAAAAAAAA , CM000663.1:g.215814204_215814205insAAAACCAACCCAACCCAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000001.9:g.213880827_213880828insAAAACCAACCCAACCCAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_009497.1:g.787552_787553insTTTGGGTTGGGTTGGTTTTTTTTTTTTTTTTTTTTTT
NG_009497.2:g.787604_787605insTTTGGGTTGGGTTGGTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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