Canonical Allele Identifier: CA2747735801
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247227_216247228del , CM000663.2:g.216247227_216247228del GRCh38
NC_000001.10:g.216420569_216420570del , CM000663.1:g.216420569_216420570del GRCh37
NC_000001.9:g.214487192_214487193del NCBI36
NG_009497.1:g.181169_181170del
NG_009497.2:g.181221_181222del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2168-2_2168-1del MANE Select ENSP00000305941.3:n.2168-2_2168-1del
ENST00000674083.1:c.2168-2_2168-1del ENSP00000501296.1:n.2168-2_2168-1del
ENST00000307340.7:c.2168-2_2168-1del ENSP00000305941.3:n.2168-2_2168-1del
ENST00000366942.3:c.2168-2_2168-1del ENSP00000355909.3:n.2168-2_2168-1del
NM_007123.5:c.2168-2_2168-1del NP_009054.5:n.2168-2_2168-1del
NM_206933.2:c.2168-2_2168-1del NP_996816.2:n.2168-2_2168-1del
NM_206933.3:c.2168-2_2168-1del NP_996816.2:n.2168-2_2168-1del
NM_007123.6:c.2168-2_2168-1del NP_009054.6:n.2168-2_2168-1del
NM_206933.4:c.2168-2_2168-1del MANE Select NP_996816.3:n.2168-2_2168-1del