Canonical Allele Identifier: CA2275253561
Gene: USH1G HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74916350C= , CM000679.2:g.74916350C= GRCh38
NC_000017.10:g.72912442C= , CM000679.1:g.72912442C= GRCh37
NC_000017.9:g.70424037C= NCBI36
NG_007882.1:g.11910G=
NG_007882.2:g.11914G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000614341.5:c.*1723G= MANE Select ENSP00000480279.1:n.*1723G=
ENST00000614341.4:c.*1723G= ENSP00000480279.1:n.*1723G=
NM_001282489.2:c.*1723G= NP_001269418.1:n.*1723G=
NM_173477.4:c.*1723G= NP_775748.2:n.*1723G=
XM_011524296.1:c.*1723G= XP_011522598.1:n.*1723G=
XM_011524296.2:c.*1723G= XP_011522598.1:n.*1723G=
NM_173477.5:c.*1723G= MANE Select NP_775748.2:n.*1723G=
NM_001282489.3:c.*1723G= NP_001269418.1:n.*1723G=