Canonical Allele Identifier: CA1220416976
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215782390_215782392delinsTAA , CM000663.2:g.215782390_215782392delinsTAA GRCh38
NC_000001.10:g.215955732_215955734delinsTAA , CM000663.1:g.215955732_215955734delinsTAA GRCh37
NC_000001.9:g.214022355_214022357delinsTAA NCBI36
NG_009497.1:g.646005_646007delinsTTA
NG_009497.2:g.646057_646059delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.10586-196_10586-194delinsTTA MANE Select ENSP00000305941.3:n.10586-196_10586-194delinsTTA
ENST00000674083.1:c.10586-196_10586-194delinsTTA ENSP00000501296.1:n.10586-196_10586-194delinsTTA
ENST00000307340.7:c.10586-196_10586-194delinsTTA ENSP00000305941.3:n.10586-196_10586-194delinsTTA
NM_206933.2:c.10586-196_10586-194delinsTTA NP_996816.2:n.10586-196_10586-194delinsTTA
NM_206933.3:c.10586-196_10586-194delinsTTA NP_996816.2:n.10586-196_10586-194delinsTTA
NM_206933.4:c.10586-196_10586-194delinsTTA MANE Select NP_996816.3:n.10586-196_10586-194delinsTTA