Canonical Allele Identifier: CA2739275641
Gene: USH2A HGNC NCBI

Linked Data

ClinVar Variation Id: 2864724
ClinVar RCV Id: RCV003697435
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216175483del , CM000663.2:g.216175483del GRCh38
NC_000001.10:g.216348825del , CM000663.1:g.216348825del GRCh37
NC_000001.9:g.214415448del NCBI36
NG_009497.1:g.252914del
NG_009497.2:g.252966del

Transcript Alleles

HGVS Amino-acid change
ENST00000307340.8:c.4397-1del MANE Select ENSP00000305941.3:n.4397-1del
ENST00000674083.1:c.4397-1del ENSP00000501296.1:n.4397-1del
ENST00000307340.7:c.4397-1del ENSP00000305941.3:n.4397-1del
ENST00000366942.3:c.4397-1del ENSP00000355909.3:n.4397-1del
NM_007123.5:c.4397-1del NP_009054.5:n.4397-1del
NM_206933.2:c.4397-1del NP_996816.2:n.4397-1del
NM_206933.3:c.4397-1del NP_996816.2:n.4397-1del
NM_007123.6:c.4397-1del NP_009054.6:n.4397-1del
NM_206933.4:c.4397-1del MANE Select NP_996816.3:n.4397-1del
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