Canonical Allele Identifier: CA2747717689
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675641_215675644del , CM000663.2:g.215675641_215675644del GRCh38
NC_000001.10:g.215848983_215848986del , CM000663.1:g.215848983_215848986del GRCh37
NC_000001.9:g.213915606_213915609del NCBI36
NG_009497.1:g.752753_752756del
NG_009497.2:g.752805_752808del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-28_12295-25del MANE Select ENSP00000305941.3:n.12295-28_12295-25del
ENST00000674083.1:c.12295-28_12295-25del ENSP00000501296.1:n.12295-28_12295-25del
ENST00000307340.7:c.12295-28_12295-25del ENSP00000305941.3:n.12295-28_12295-25del
NM_206933.2:c.12295-28_12295-25del NP_996816.2:n.12295-28_12295-25del
NM_206933.3:c.12295-28_12295-25del NP_996816.2:n.12295-28_12295-25del
NM_206933.4:c.12295-28_12295-25del MANE Select NP_996816.3:n.12295-28_12295-25del