Canonical Allele Identifier: CA1220373990
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675592_215675593delinsAC , CM000663.2:g.215675592_215675593delinsAC GRCh38
NC_000001.10:g.215848934_215848935delinsAC , CM000663.1:g.215848934_215848935delinsAC GRCh37
NC_000001.9:g.213915557_213915558delinsAC NCBI36
NG_009497.1:g.752804_752805delinsGT
NG_009497.2:g.752856_752857delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12318_12319delinsGT MANE Select ENSP00000305941.3:p.Gly4106=
ENST00000674083.1:c.12318_12319delinsGT ENSP00000501296.1:p.Gly4106=
ENST00000307340.7:c.12318_12319delinsGT ENSP00000305941.3:p.Gly4106=
NM_206933.2:c.12318_12319delinsGT NP_996816.2:p.Gly4106=
NM_206933.3:c.12318_12319delinsGT NP_996816.2:p.Gly4106=
NM_206933.4:c.12318_12319delinsGT MANE Select NP_996816.3:p.Gly4106=