Canonical Allele Identifier: CA1220455713
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867169_215867170delinsAC , CM000663.2:g.215867169_215867170delinsAC GRCh38
NC_000001.10:g.216040511_216040512delinsAC , CM000663.1:g.216040511_216040512delinsAC GRCh37
NC_000001.9:g.214107134_214107135delinsAC NCBI36
NG_009497.1:g.561227_561228delinsGT
NG_009497.2:g.561279_561280delinsGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8682_8683delinsGT MANE Select ENSP00000305941.3:p.Arg2894=
ENST00000674083.1:c.8682_8683delinsGT ENSP00000501296.1:p.Arg2894=
ENST00000307340.7:c.8682_8683delinsGT ENSP00000305941.3:p.Arg2894=
NM_206933.2:c.8682_8683delinsGT NP_996816.2:p.Arg2894=
NM_206933.3:c.8682_8683delinsGT NP_996816.2:p.Arg2894=
NM_206933.4:c.8682_8683delinsGT MANE Select NP_996816.3:p.Arg2894=