Canonical Allele Identifier: CA2275253568

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74916370T= , CM000679.2:g.74916370T=	GRCh38
NC_000017.10:g.72912462T= , CM000679.1:g.72912462T=	GRCh37
NC_000017.9:g.70424057T=	NCBI36
NG_007882.1:g.11890A=
NG_007882.2:g.11894A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000614341.5:c.*1703A= MANE Select	ENSP00000480279.1:n.*1703A=
ENST00000614341.4:c.*1703A=	ENSP00000480279.1:n.*1703A=
NM_001282489.2:c.*1703A=	NP_001269418.1:n.*1703A=
NM_173477.4:c.*1703A=	NP_775748.2:n.*1703A=
XM_011524296.1:c.*1703A=	XP_011522598.1:n.*1703A=
XM_011524296.2:c.*1703A=	XP_011522598.1:n.*1703A=
NM_173477.5:c.*1703A= MANE Select	NP_775748.2:n.*1703A=
NM_001282489.3:c.*1703A=	NP_001269418.1:n.*1703A=