Canonical Allele Identifier: CA2275255144
Gene: USH1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74919557G= , CM000679.2:g.74919557G= GRCh38
NC_000017.10:g.72915652G= , CM000679.1:g.72915652G= GRCh37
NC_000017.9:g.70427247G= NCBI36
NG_007882.1:g.8700C=
NG_033062.1:g.283G=
NG_007882.2:g.8707C=
NG_033062.2:g.283G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.1279C= MANE Select ENSP00000480279.1:p.Arg427=
ENST00000579243.1:c.*878C= ENSP00000462568.1:n.*878C=
ENST00000614341.4:c.1279C= ENSP00000480279.1:p.Arg427=
NM_001282489.2:c.970C= NP_001269418.1:p.Arg324=
NM_173477.4:c.1279C= NP_775748.2:p.Arg427=
XM_011524296.1:c.970C= XP_011522598.1:p.Arg324=
XM_011524296.2:c.970C= XP_011522598.1:p.Arg324=
NM_173477.5:c.1279C= MANE Select NP_775748.2:p.Arg427=
NM_001282489.3:c.970C= NP_001269418.1:p.Arg324=