Canonical Allele Identifier: CA775051394
Gene: USH1G HGNC NCBI

Linked Data

dbSNP Id: rs1290462412
MyVariant Identifiers: chr17:g.72912448A>T (hg19) chr17:g.74916356A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74916356A>T , CM000679.2:g.74916356A>T GRCh38
NC_000017.10:g.72912448A>T , CM000679.1:g.72912448A>T GRCh37
NC_000017.9:g.70424043A>T NCBI36
NG_007882.1:g.11904T>A
NG_007882.2:g.11908T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.*1717T>A MANE Select ENSP00000480279.1:n.*1717T>A
ENST00000614341.4:c.*1717T>A ENSP00000480279.1:n.*1717T>A
NM_001282489.2:c.*1717T>A NP_001269418.1:n.*1717T>A
NM_173477.4:c.*1717T>A NP_775748.2:n.*1717T>A
XM_011524296.1:c.*1717T>A XP_011522598.1:n.*1717T>A
XM_011524296.2:c.*1717T>A XP_011522598.1:n.*1717T>A
NM_173477.5:c.*1717T>A MANE Select NP_775748.2:n.*1717T>A
NM_001282489.3:c.*1717T>A NP_001269418.1:n.*1717T>A
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