Canonical Allele Identifier: CA1220373852
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675212_215675214delinsCCA , CM000663.2:g.215675212_215675214delinsCCA GRCh38
NC_000001.10:g.215848554_215848556delinsCCA , CM000663.1:g.215848554_215848556delinsCCA GRCh37
NC_000001.9:g.213915177_213915179delinsCCA NCBI36
NG_009497.1:g.753183_753185delinsTGG
NG_009497.2:g.753235_753237delinsTGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12697_12699delinsTGG MANE Select ENSP00000305941.3:p.Trp4233=
ENST00000674083.1:c.12697_12699delinsTGG ENSP00000501296.1:p.Trp4233=
ENST00000307340.7:c.12697_12699delinsTGG ENSP00000305941.3:p.Trp4233=
NM_206933.2:c.12697_12699delinsTGG NP_996816.2:p.Trp4233=
NM_206933.3:c.12697_12699delinsTGG NP_996816.2:p.Trp4233=
NM_206933.4:c.12697_12699delinsTGG MANE Select NP_996816.3:p.Trp4233=