Canonical Allele Identifier: CA2275255212
Gene: USH1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74919689C= , CM000679.2:g.74919689C= GRCh38
NC_000017.10:g.72915784C= , CM000679.1:g.72915784C= GRCh37
NC_000017.9:g.70427379C= NCBI36
NG_007882.1:g.8568G=
NG_033062.1:g.415C=
NG_007882.2:g.8575G=
NG_033062.2:g.415C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.1147G= MANE Select ENSP00000480279.1:p.Glu383=
ENST00000579243.1:c.*746G= ENSP00000462568.1:n.*746G=
ENST00000614341.4:c.1147G= ENSP00000480279.1:p.Glu383=
NM_001282489.2:c.838G= NP_001269418.1:p.Glu280=
NM_173477.4:c.1147G= NP_775748.2:p.Glu383=
XM_011524296.1:c.838G= XP_011522598.1:p.Glu280=
XM_011524296.2:c.838G= XP_011522598.1:p.Glu280=
NM_173477.5:c.1147G= MANE Select NP_775748.2:p.Glu383=
NM_001282489.3:c.838G= NP_001269418.1:p.Glu280=