Canonical Allele Identifier: CA1012185286
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640862_215640863insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000663.2:g.215640862_215640863insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000001.10:g.215814204_215814205insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000663.1:g.215814204_215814205insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000001.9:g.213880827_213880828insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_009497.1:g.787552_787553insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NG_009497.2:g.787604_787605insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

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