Canonical Allele Identifier: CA1220373952
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675501_215675502delinsCT , CM000663.2:g.215675501_215675502delinsCT GRCh38
NC_000001.10:g.215848843_215848844delinsCT , CM000663.1:g.215848843_215848844delinsCT GRCh37
NC_000001.9:g.213915466_213915467delinsCT NCBI36
NG_009497.1:g.752895_752896delinsAG
NG_009497.2:g.752947_752948delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12409_12410delinsAG MANE Select ENSP00000305941.3:p.Arg4137=
ENST00000674083.1:c.12409_12410delinsAG ENSP00000501296.1:p.Arg4137=
ENST00000307340.7:c.12409_12410delinsAG ENSP00000305941.3:p.Arg4137=
NM_206933.2:c.12409_12410delinsAG NP_996816.2:p.Arg4137=
NM_206933.3:c.12409_12410delinsAG NP_996816.2:p.Arg4137=
NM_206933.4:c.12409_12410delinsAG MANE Select NP_996816.3:p.Arg4137=