Canonical Allele Identifier: CA2747721894
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215799191_215799198del , CM000663.2:g.215799191_215799198del GRCh38
NC_000001.10:g.215972533_215972540del , CM000663.1:g.215972533_215972540del GRCh37
NC_000001.9:g.214039156_214039163del NCBI36
NG_009497.1:g.629199_629206del
NG_009497.2:g.629251_629258del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.9740-73_9740-66del MANE Select ENSP00000305941.3:n.9740-73_9740-66del
ENST00000674083.1:c.9740-73_9740-66del ENSP00000501296.1:n.9740-73_9740-66del
ENST00000307340.7:c.9740-73_9740-66del ENSP00000305941.3:n.9740-73_9740-66del
NM_206933.2:c.9740-73_9740-66del NP_996816.2:n.9740-73_9740-66del
NM_206933.3:c.9740-73_9740-66del NP_996816.2:n.9740-73_9740-66del
NM_206933.4:c.9740-73_9740-66del MANE Select NP_996816.3:n.9740-73_9740-66del