Canonical Allele Identifier: CA1393460
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 1413840
ClinVar RCV Id: RCV001928349
dbSNP Id: rs773417196

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215675442dup , CM000663.2:g.215675442dup GRCh38
NC_000001.10:g.215848784dup , CM000663.1:g.215848784dup GRCh37
NC_000001.9:g.213915407dup NCBI36
NG_009497.1:g.752955dup
NG_009497.2:g.753007dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.12469dup MANE Select ENSP00000305941.3:p.Ser4157PhefsTer16
ENST00000674083.1:c.12469dup ENSP00000501296.1:p.Ser4157PhefsTer16
ENST00000307340.7:c.12469dup ENSP00000305941.3:p.Ser4157PhefsTer16
NM_206933.2:c.12469dup NP_996816.2:p.Ser4157PhefsTer16
NM_206933.3:c.12469dup NP_996816.2:p.Ser4157PhefsTer16
NM_206933.4:c.12469dup MANE Select NP_996816.3:p.Ser4157PhefsTer16