Canonical Allele Identifier: CA2275255234
Gene: USH1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74919733C= , CM000679.2:g.74919733C= GRCh38
NC_000017.10:g.72915828C= , CM000679.1:g.72915828C= GRCh37
NC_000017.9:g.70427423C= NCBI36
NG_007882.1:g.8524G=
NG_033062.1:g.459C=
NG_007882.2:g.8531G=
NG_033062.2:g.459C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.1103G= MANE Select ENSP00000480279.1:p.Cys368=
ENST00000579243.1:c.*702G= ENSP00000462568.1:n.*702G=
ENST00000614341.4:c.1103G= ENSP00000480279.1:p.Cys368=
NM_001282489.2:c.794G= NP_001269418.1:p.Cys265=
NM_173477.4:c.1103G= NP_775748.2:p.Cys368=
XM_011524296.1:c.794G= XP_011522598.1:p.Cys265=
XM_011524296.2:c.794G= XP_011522598.1:p.Cys265=
NM_173477.5:c.1103G= MANE Select NP_775748.2:p.Cys368=
NM_001282489.3:c.794G= NP_001269418.1:p.Cys265=