Canonical Allele Identifier: CA2650499657
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215640862_215640863insAAAACAAACAAAACCATCCCAAACAAAAAAAAAAAAAAA , CM000663.2:g.215640862_215640863insAAAACAAACAAAACCATCCCAAACAAAAAAAAAAAAAAA GRCh38
NC_000001.10:g.215814204_215814205insAAAACAAACAAAACCATCCCAAACAAAAAAAAAAAAAAA , CM000663.1:g.215814204_215814205insAAAACAAACAAAACCATCCCAAACAAAAAAAAAAAAAAA GRCh37
NC_000001.9:g.213880827_213880828insAAAACAAACAAAACCATCCCAAACAAAAAAAAAAAAAAA NCBI36
NG_009497.1:g.787549_787550insGTTTGGGATGGTTTTGTTTGTTTTTTTTTTTTTTTTTTT
NG_009497.2:g.787601_787602insGTTTGGGATGGTTTTGTTTGTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.14792-114_14792-113insGTTTGGGATGGTTTTGTTTGTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000305941.3:n.14792-114_14792-113insGTTTGGGATGGTTTTGTTT...
ENST00000674083.1:c.14792-114_14792-113insGTTTGGGATGGTTTTGTTTGTTTTTTTTTTTTTTTTTTT ENSP00000501296.1:n.14792-114_14792-113insGTTTGGGATGGTTTTGTTT...
ENST00000307340.7:c.14792-114_14792-113insGTTTGGGATGGTTTTGTTTGTTTTTTTTTTTTTTTTTTT ENSP00000305941.3:n.14792-114_14792-113insGTTTGGGATGGTTTTGTTT...
NM_206933.2:c.14792-114_14792-113insGTTTGGGATGGTTTTGTTTGTTTTTTTTTTTTTTTTTTT NP_996816.2:n.14792-114_14792-113insGTTTGGGATGGTTTTGTTTGTTTTT...
NM_206933.3:c.14792-114_14792-113insGTTTGGGATGGTTTTGTTTGTTTTTTTTTTTTTTTTTTT NP_996816.2:n.14792-114_14792-113insGTTTGGGATGGTTTTGTTTGTTTTT...
NM_206933.4:c.14792-114_14792-113insGTTTGGGATGGTTTTGTTTGTTTTTTTTTTTTTTTTTTT MANE Select NP_996816.3:n.14792-114_14792-113insGTTTGGGATGGTTTTGTTTGTTTTT...