Canonical Allele Identifier: CA913072831
Gene: USH2A HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.216420421_216420424del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216247079_216247082del , CM000663.2:g.216247079_216247082del GRCh38
NC_000001.10:g.216420421_216420424del , CM000663.1:g.216420421_216420424del GRCh37
NC_000001.9:g.214487044_214487047del NCBI36
NG_009497.1:g.181315_181318del
NG_009497.2:g.181367_181370del

Transcript Alleles

HGVS Amino-acid Change
ENST00000307340.8:c.2312_2315del MANE Select ENSP00000305941.3:p.Glu771AlafsTer16
ENST00000674083.1:c.2312_2315del ENSP00000501296.1:p.Glu771AlafsTer16
ENST00000307340.7:c.2312_2315del ENSP00000305941.3:p.Glu771AlafsTer16
ENST00000366942.3:c.2312_2315del ENSP00000355909.3:p.Glu771AlafsTer16
NM_007123.5:c.2312_2315del NP_009054.5:p.Glu771AlafsTer16
NM_206933.2:c.2312_2315del NP_996816.2:p.Glu771AlafsTer16
NM_206933.3:c.2312_2315del NP_996816.2:p.Glu771AlafsTer16
NM_007123.6:c.2312_2315del NP_009054.6:p.Glu771AlafsTer16
NM_206933.4:c.2312_2315del MANE Select NP_996816.3:p.Glu771AlafsTer16
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