Canonical Allele Identifier: CA2747720808
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215780141_215780142insA , CM000663.2:g.215780141_215780142insA GRCh38
NC_000001.10:g.215953483_215953484insA , CM000663.1:g.215953483_215953484insA GRCh37
NC_000001.9:g.214020106_214020107insA NCBI36
NG_009497.1:g.648255_648256insT
NG_009497.2:g.648307_648308insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10741-101_10741-100insT MANE Select ENSP00000305941.3:n.10741-101_10741-100insT
ENST00000674083.1:c.10741-101_10741-100insT ENSP00000501296.1:n.10741-101_10741-100insT
ENST00000307340.7:c.10741-101_10741-100insT ENSP00000305941.3:n.10741-101_10741-100insT
NM_206933.2:c.10741-101_10741-100insT NP_996816.2:n.10741-101_10741-100insT
NM_206933.3:c.10741-101_10741-100insT NP_996816.2:n.10741-101_10741-100insT
NM_206933.4:c.10741-101_10741-100insT MANE Select NP_996816.3:n.10741-101_10741-100insT