Canonical Allele Identifier: CA400961457
Gene: USH1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74919631T>G , CM000679.2:g.74919631T>G GRCh38
NC_000017.10:g.72915726T>G , CM000679.1:g.72915726T>G GRCh37
NC_000017.9:g.70427321T>G NCBI36
NG_007882.1:g.8626A>C
NG_033062.1:g.357T>G
NG_007882.2:g.8633A>C
NG_033062.2:g.357T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.1205A>C MANE Select ENSP00000480279.1:p.Glu402Ala
ENST00000579243.1:c.*804A>C ENSP00000462568.1:n.*804A>C
ENST00000614341.4:c.1205A>C ENSP00000480279.1:p.Glu402Ala
NM_001282489.2:c.896A>C NP_001269418.1:p.Glu299Ala
NM_173477.4:c.1205A>C NP_775748.2:p.Glu402Ala
XM_011524296.1:c.896A>C XP_011522598.1:p.Glu299Ala
XM_011524296.2:c.896A>C XP_011522598.1:p.Glu299Ala
NM_173477.5:c.1205A>C MANE Select NP_775748.2:p.Glu402Ala
NM_001282489.3:c.896A>C NP_001269418.1:p.Glu299Ala