Canonical Allele Identifier: CA2650527156
Gene: USH2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215782331_215782332insTGAGACAGCAATATAATAG , CM000663.2:g.215782331_215782332insTGAGACAGCAATATAATAG GRCh38
NC_000001.10:g.215955673_215955674insTGAGACAGCAATATAATAG , CM000663.1:g.215955673_215955674insTGAGACAGCAATATAATAG GRCh37
NC_000001.9:g.214022296_214022297insTGAGACAGCAATATAATAG NCBI36
NG_009497.1:g.646065_646066insCTATTATATTGCTGTCTCA
NG_009497.2:g.646117_646118insCTATTATATTGCTGTCTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10586-136_10586-135insCTATTATATTGCTGTCTCA MANE Select ENSP00000305941.3:n.10586-136_10586-135insCTATTATATTGCTGTCTCA...
ENST00000674083.1:c.10586-136_10586-135insCTATTATATTGCTGTCTCA ENSP00000501296.1:n.10586-136_10586-135insCTATTATATTGCTGTCTCA...
ENST00000307340.7:c.10586-136_10586-135insCTATTATATTGCTGTCTCA ENSP00000305941.3:n.10586-136_10586-135insCTATTATATTGCTGTCTCA...
NM_206933.2:c.10586-136_10586-135insCTATTATATTGCTGTCTCA NP_996816.2:n.10586-136_10586-135insCTATTATATTGCTGTCTCA
NM_206933.3:c.10586-136_10586-135insCTATTATATTGCTGTCTCA NP_996816.2:n.10586-136_10586-135insCTATTATATTGCTGTCTCA
NM_206933.4:c.10586-136_10586-135insCTATTATATTGCTGTCTCA MANE Select NP_996816.3:n.10586-136_10586-135insCTATTATATTGCTGTCTCA