Canonical Allele Identifier: CA2275253559
Gene: USH1G HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74916343_74916347delinsTGGCA , CM000679.2:g.74916343_74916347delinsTGGCA GRCh38
NC_000017.10:g.72912435_72912439delinsTGGCA , CM000679.1:g.72912435_72912439delinsTGGCA GRCh37
NC_000017.9:g.70424030_70424034delinsTGGCA NCBI36
NG_007882.1:g.11913_11917delinsTGCCA
NG_007882.2:g.11917_11921delinsTGCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.*1726_*1730delinsTGCCA MANE Select ENSP00000480279.1:n.*1726_*1730delinsTGCCA
ENST00000614341.4:c.*1726_*1730delinsTGCCA ENSP00000480279.1:n.*1726_*1730delinsTGCCA
NM_001282489.2:c.*1726_*1730delinsTGCCA NP_001269418.1:n.*1726_*1730delinsTGCCA
NM_173477.4:c.*1726_*1730delinsTGCCA NP_775748.2:n.*1726_*1730delinsTGCCA
XM_011524296.1:c.*1726_*1730delinsTGCCA XP_011522598.1:n.*1726_*1730delinsTGCCA
XM_011524296.2:c.*1726_*1730delinsTGCCA XP_011522598.1:n.*1726_*1730delinsTGCCA
NM_173477.5:c.*1726_*1730delinsTGCCA MANE Select NP_775748.2:n.*1726_*1730delinsTGCCA
NM_001282489.3:c.*1726_*1730delinsTGCCA NP_001269418.1:n.*1726_*1730delinsTGCCA
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