Canonical Allele Identifier: CA1220455625
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1664484859

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215866942_215866945del , CM000663.2:g.215866942_215866945del GRCh38
NC_000001.10:g.216040284_216040287del , CM000663.1:g.216040284_216040287del GRCh37
NC_000001.9:g.214106907_214106910del NCBI36
NG_009497.1:g.561453_561456del
NG_009497.2:g.561505_561508del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8845+63_8845+66del MANE Select ENSP00000305941.3:n.8845+63_8845+66del
ENST00000674083.1:c.8845+63_8845+66del ENSP00000501296.1:n.8845+63_8845+66del
ENST00000307340.7:c.8845+63_8845+66del ENSP00000305941.3:n.8845+63_8845+66del
NM_206933.2:c.8845+63_8845+66del NP_996816.2:n.8845+63_8845+66del
NM_206933.3:c.8845+63_8845+66del NP_996816.2:n.8845+63_8845+66del
NM_206933.4:c.8845+63_8845+66del MANE Select NP_996816.3:n.8845+63_8845+66del