Canonical Allele Identifier: CA731337821
Gene: USH2A HGNC NCBI

Linked Data

dbSNP Id: rs1376040005

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675645_215675648del , CM000663.2:g.215675645_215675648del GRCh38
NC_000001.10:g.215848987_215848990del , CM000663.1:g.215848987_215848990del GRCh37
NC_000001.9:g.213915610_213915613del NCBI36
NG_009497.1:g.752749_752752del
NG_009497.2:g.752801_752804del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-32_12295-29del MANE Select ENSP00000305941.3:n.12295-32_12295-29del
ENST00000674083.1:c.12295-32_12295-29del ENSP00000501296.1:n.12295-32_12295-29del
ENST00000307340.7:c.12295-32_12295-29del ENSP00000305941.3:n.12295-32_12295-29del
NM_206933.2:c.12295-32_12295-29del NP_996816.2:n.12295-32_12295-29del
NM_206933.3:c.12295-32_12295-29del NP_996816.2:n.12295-32_12295-29del
NM_206933.4:c.12295-32_12295-29del MANE Select NP_996816.3:n.12295-32_12295-29del