Canonical Allele Identifier: CA731342440
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1218282893

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728572_215728573del , CM000663.2:g.215728572_215728573del GRCh38
NC_000001.10:g.215901914_215901915del , CM000663.1:g.215901914_215901915del GRCh37
NC_000001.9:g.213968537_213968538del NCBI36
NG_009497.1:g.699825_699826del
NG_009497.2:g.699877_699878del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-188_11712-187del MANE Select ENSP00000305941.3:n.11712-188_11712-187del
ENST00000674083.1:c.11712-188_11712-187del ENSP00000501296.1:n.11712-188_11712-187del
ENST00000307340.7:c.11712-188_11712-187del ENSP00000305941.3:n.11712-188_11712-187del
NM_206933.2:c.11712-188_11712-187del NP_996816.2:n.11712-188_11712-187del
NM_206933.3:c.11712-188_11712-187del NP_996816.2:n.11712-188_11712-187del
NM_206933.4:c.11712-188_11712-187del MANE Select NP_996816.3:n.11712-188_11712-187del