Canonical Allele Identifier: CA731342501
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1311988583

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215728605_215728606del , CM000663.2:g.215728605_215728606del GRCh38
NC_000001.10:g.215901947_215901948del , CM000663.1:g.215901947_215901948del GRCh37
NC_000001.9:g.213968570_213968571del NCBI36
NG_009497.1:g.699813_699814del
NG_009497.2:g.699865_699866del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.11712-200_11712-199del MANE Select ENSP00000305941.3:n.11712-200_11712-199del
ENST00000674083.1:c.11712-200_11712-199del ENSP00000501296.1:n.11712-200_11712-199del
ENST00000307340.7:c.11712-200_11712-199del ENSP00000305941.3:n.11712-200_11712-199del
NM_206933.2:c.11712-200_11712-199del NP_996816.2:n.11712-200_11712-199del
NM_206933.3:c.11712-200_11712-199del NP_996816.2:n.11712-200_11712-199del
NM_206933.4:c.11712-200_11712-199del MANE Select NP_996816.3:n.11712-200_11712-199del