Canonical Allele Identifier: CA1220412652
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215766666_215766667delinsAT , CM000663.2:g.215766666_215766667delinsAT GRCh38
NC_000001.10:g.215940008_215940009delinsAT , CM000663.1:g.215940008_215940009delinsAT GRCh37
NC_000001.9:g.214006631_214006632delinsAT NCBI36
NG_009497.1:g.661730_661731delinsAT
NG_009497.2:g.661782_661783delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.11047+14_11047+15delinsAT MANE Select ENSP00000305941.3:n.11047+14_11047+15deli...
ENST00000674083.1:c.11047+14_11047+15delinsAT ENSP00000501296.1:n.11047+14_11047+15deli...
ENST00000307340.7:c.11047+14_11047+15delinsAT ENSP00000305941.3:n.11047+14_11047+15deli...
NM_206933.2:c.11047+14_11047+15delinsAT NP_996816.2:n.11047+14_11047+15delinsAT
NM_206933.3:c.11047+14_11047+15delinsAT NP_996816.2:n.11047+14_11047+15delinsAT
NM_206933.4:c.11047+14_11047+15delinsAT MANE Select NP_996816.3:n.11047+14_11047+15delinsAT