Canonical Allele Identifier: CA1220373961
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675516_215675517delinsAG , CM000663.2:g.215675516_215675517delinsAG GRCh38
NC_000001.10:g.215848858_215848859delinsAG , CM000663.1:g.215848858_215848859delinsAG GRCh37
NC_000001.9:g.213915481_213915482delinsAG NCBI36
NG_009497.1:g.752880_752881delinsCT
NG_009497.2:g.752932_752933delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12394_12395delinsCT MANE Select ENSP00000305941.3:p.Leu4132=
ENST00000674083.1:c.12394_12395delinsCT ENSP00000501296.1:p.Leu4132=
ENST00000307340.7:c.12394_12395delinsCT ENSP00000305941.3:p.Leu4132=
NM_206933.2:c.12394_12395delinsCT NP_996816.2:p.Leu4132=
NM_206933.3:c.12394_12395delinsCT NP_996816.2:p.Leu4132=
NM_206933.4:c.12394_12395delinsCT MANE Select NP_996816.3:p.Leu4132=