Canonical Allele Identifier: CA2747717698
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675650_215675655del , CM000663.2:g.215675650_215675655del GRCh38
NC_000001.10:g.215848992_215848997del , CM000663.1:g.215848992_215848997del GRCh37
NC_000001.9:g.213915615_213915620del NCBI36
NG_009497.1:g.752742_752747del
NG_009497.2:g.752794_752799del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12295-39_12295-34del MANE Select ENSP00000305941.3:n.12295-39_12295-34del
ENST00000674083.1:c.12295-39_12295-34del ENSP00000501296.1:n.12295-39_12295-34del
ENST00000307340.7:c.12295-39_12295-34del ENSP00000305941.3:n.12295-39_12295-34del
NM_206933.2:c.12295-39_12295-34del NP_996816.2:n.12295-39_12295-34del
NM_206933.3:c.12295-39_12295-34del NP_996816.2:n.12295-39_12295-34del
NM_206933.4:c.12295-39_12295-34del MANE Select NP_996816.3:n.12295-39_12295-34del