Canonical Allele Identifier: CA2275255338

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919912G= , CM000679.2:g.74919912G=	GRCh38
NC_000017.10:g.72916007G= , CM000679.1:g.72916007G=	GRCh37
NC_000017.9:g.70427602G=	NCBI36
NG_007882.1:g.8345C=
NG_033062.1:g.638G=
NG_007882.2:g.8352C=
NG_033062.2:g.638G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000614341.5:c.924C= MANE Select	ENSP00000480279.1:p.Thr308=
ENST00000579243.1:c.*523C=	ENSP00000462568.1:n.*523C=
ENST00000614341.4:c.924C=	ENSP00000480279.1:p.Thr308=
NM_001282489.2:c.615C=	NP_001269418.1:p.Thr205=
NM_173477.4:c.924C=	NP_775748.2:p.Thr308=
XM_011524296.1:c.615C=	XP_011522598.1:p.Thr205=
XM_011524296.2:c.615C=	XP_011522598.1:p.Thr205=
NM_173477.5:c.924C= MANE Select	NP_775748.2:p.Thr308=
NM_001282489.3:c.615C=	NP_001269418.1:p.Thr205=