Canonical Allele Identifier: CA1220455681
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215867092_215867095delinsCGTT , CM000663.2:g.215867092_215867095delinsCGTT GRCh38
NC_000001.10:g.216040434_216040437delinsCGTT , CM000663.1:g.216040434_216040437delinsCGTT GRCh37
NC_000001.9:g.214107057_214107060delinsCGTT NCBI36
NG_009497.1:g.561302_561305delinsAACG
NG_009497.2:g.561354_561357delinsAACG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.8757_8760delinsAACG MANE Select ENSP00000305941.3:p.Thr2919=
ENST00000674083.1:c.8757_8760delinsAACG ENSP00000501296.1:p.Thr2919=
ENST00000307340.7:c.8757_8760delinsAACG ENSP00000305941.3:p.Thr2919=
NM_206933.2:c.8757_8760delinsAACG NP_996816.2:p.Thr2919=
NM_206933.3:c.8757_8760delinsAACG NP_996816.2:p.Thr2919=
NM_206933.4:c.8757_8760delinsAACG MANE Select NP_996816.3:p.Thr2919=