Canonical Allele Identifier: CA2275256748

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74922751G= , CM000679.2:g.74922751G=	GRCh38
NC_000017.10:g.72918846G= , CM000679.1:g.72918846G=	GRCh37
NC_000017.9:g.70430441G=	NCBI36
NG_007882.1:g.5506C=
NG_033062.1:g.3477G=
NG_007882.2:g.5513C=
NG_033062.2:g.3477G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.164+159C= MANE Select	ENSP00000480279.1:n.164+159C=
ENST00000579243.1:c.164+159C=	ENSP00000462568.1:n.164+159C=
ENST00000614341.4:c.164+159C=	ENSP00000480279.1:n.164+159C=
NM_001282489.2:c.-93+159C=	NP_001269418.1:n.-93+159C=
NM_173477.4:c.164+159C=	NP_775748.2:n.164+159C=
XM_011524296.1:c.-321C=	XP_011522598.1:n.-321C=
XM_011524296.2:c.-321C=	XP_011522598.1:n.-321C=
NM_173477.5:c.164+159C= MANE Select	NP_775748.2:n.164+159C=
NM_001282489.3:c.-93+159C=	NP_001269418.1:n.-93+159C=