Canonical Allele Identifier: CA2695199997
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2679519
ClinVar RCV Id: RCV003464822

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867171_215867173delinsTT , CM000663.2:g.215867171_215867173delinsTT GRCh38
NC_000001.10:g.216040513_216040515delinsTT , CM000663.1:g.216040513_216040515delinsTT GRCh37
NC_000001.9:g.214107136_214107138delinsTT NCBI36
NG_009497.1:g.561224_561226delinsAA
NG_009497.2:g.561276_561278delinsAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8682-3_8682-1delinsAA MANE Select ENSP00000305941.3:n.8682-3_8682-1delinsAA
ENST00000674083.1:c.8682-3_8682-1delinsAA ENSP00000501296.1:n.8682-3_8682-1delinsAA
ENST00000307340.7:c.8682-3_8682-1delinsAA ENSP00000305941.3:n.8682-3_8682-1delinsAA
NM_206933.2:c.8682-3_8682-1delinsAA NP_996816.2:n.8682-3_8682-1delinsAA
NM_206933.3:c.8682-3_8682-1delinsAA NP_996816.2:n.8682-3_8682-1delinsAA
NM_206933.4:c.8682-3_8682-1delinsAA MANE Select NP_996816.3:n.8682-3_8682-1delinsAA