Canonical Allele Identifier: CA2747720750
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780108_215780109insACA , CM000663.2:g.215780108_215780109insACA GRCh38
NC_000001.10:g.215953450_215953451insACA , CM000663.1:g.215953450_215953451insACA GRCh37
NC_000001.9:g.214020073_214020074insACA NCBI36
NG_009497.1:g.648288_648289insTGT
NG_009497.2:g.648340_648341insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-68_10741-67insTGT MANE Select ENSP00000305941.3:n.10741-68_10741-67insTGT
ENST00000674083.1:c.10741-68_10741-67insTGT ENSP00000501296.1:n.10741-68_10741-67insTGT
ENST00000307340.7:c.10741-68_10741-67insTGT ENSP00000305941.3:n.10741-68_10741-67insTGT
NM_206933.2:c.10741-68_10741-67insTGT NP_996816.2:n.10741-68_10741-67insTGT
NM_206933.3:c.10741-68_10741-67insTGT NP_996816.2:n.10741-68_10741-67insTGT
NM_206933.4:c.10741-68_10741-67insTGT MANE Select NP_996816.3:n.10741-68_10741-67insTGT