Canonical Allele Identifier: CA423426586
Gene: USH2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.215844604del (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.215671264del , CM000663.2:g.215671264del GRCh38
NC_000001.10:g.215844606del , CM000663.1:g.215844606del GRCh37
NC_000001.9:g.213911229del NCBI36
NG_009497.1:g.757135del
NG_009497.2:g.757187del

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.13843del MANE Select ENSP00000305941.3:p.Leu4615TrpfsTer19
ENST00000674083.1:c.13843del ENSP00000501296.1:p.Leu4615TrpfsTer19
ENST00000307340.7:c.13843del ENSP00000305941.3:p.Leu4615TrpfsTer19
NM_206933.2:c.13843del NP_996816.2:p.Leu4615TrpfsTer19
NM_206933.3:c.13843del NP_996816.2:p.Leu4615TrpfsTer19
NM_206933.4:c.13843del MANE Select NP_996816.3:p.Leu4615TrpfsTer19