Canonical Allele Identifier: CA2960079003
Community Standard Title: NM_206933.4(USH2A):c.14391dup (p.Phe4798LeufsTer3)
Gene: USH2A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215648720dup , CM000663.2:g.215648720dup GRCh38
NC_000001.10:g.215822062dup , CM000663.1:g.215822062dup GRCh37
NC_000001.9:g.213888685dup NCBI36
NG_009497.1:g.779678dup
NG_009497.2:g.779730dup

Transcript Alleles

HGVS Amino-acid Change
NM_206933.4:c.14391dup MANE Select NP_996816.3:p.Phe4798LeufsTer3
ENST00000307340.8:c.14391dup MANE Select ENSP00000305941.3:p.Phe4798LeufsTer3
NM_206933.2:c.14391dup NP_996816.2:p.Phe4798LeufsTer3
NM_206933.3:c.14391dup NP_996816.2:p.Phe4798LeufsTer3
ENST00000307340.7:c.14391dup ENSP00000305941.3:p.Phe4798LeufsTer3
ENST00000674083.1:c.14391dup ENSP00000501296.1:p.Phe4798LeufsTer3