Canonical Allele Identifier: CA400963767
Gene: USH1G HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74920130C>A , CM000679.2:g.74920130C>A GRCh38
NC_000017.10:g.72916225C>A , CM000679.1:g.72916225C>A GRCh37
NC_000017.9:g.70427820C>A NCBI36
NG_007882.1:g.8127G>T
NG_033062.1:g.856C>A
NG_007882.2:g.8134G>T
NG_033062.2:g.856C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.706G>T MANE Select ENSP00000480279.1:p.Asp236Tyr
ENST00000579243.1:c.*305G>T ENSP00000462568.1:n.*305G>T
ENST00000614341.4:c.706G>T ENSP00000480279.1:p.Asp236Tyr
NM_001282489.2:c.397G>T NP_001269418.1:p.Asp133Tyr
NM_173477.4:c.706G>T NP_775748.2:p.Asp236Tyr
XM_011524296.1:c.397G>T XP_011522598.1:p.Asp133Tyr
XM_011524296.2:c.397G>T XP_011522598.1:p.Asp133Tyr
NM_173477.5:c.706G>T MANE Select NP_775748.2:p.Asp236Tyr
NM_001282489.3:c.397G>T NP_001269418.1:p.Asp133Tyr