Canonical Allele Identifier: CA293981857
Gene: USH1G HGNC NCBI

Linked Data

dbSNP Id: rs35184411
MyVariant Identifiers: chr17:g.72913372del (hg19) chr17:g.74917278del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74917279del , CM000679.2:g.74917279del GRCh38
NC_000017.10:g.72913373del , CM000679.1:g.72913373del GRCh37
NC_000017.9:g.70424968del NCBI36
NG_007882.1:g.10980del
NG_007882.2:g.10986del

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.*795del MANE Select ENSP00000480279.1:n.*795del
ENST00000614341.4:c.*795del ENSP00000480279.1:n.*795del
NM_001282489.2:c.*795del NP_001269418.1:n.*795del
NM_173477.4:c.*795del NP_775748.2:n.*795del
XM_011524296.1:c.*795del XP_011522598.1:n.*795del
XM_011524296.2:c.*795del XP_011522598.1:n.*795del
NM_173477.5:c.*795del MANE Select NP_775748.2:n.*795del
NM_001282489.3:c.*795del NP_001269418.1:n.*795del
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