Canonical Allele Identifier: CA2275256744

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74922742G= , CM000679.2:g.74922742G=	GRCh38
NC_000017.10:g.72918837G= , CM000679.1:g.72918837G=	GRCh37
NC_000017.9:g.70430432G=	NCBI36
NG_007882.1:g.5515C=
NG_033062.1:g.3468G=
NG_007882.2:g.5522C=
NG_033062.2:g.3468G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.164+168C= MANE Select	ENSP00000480279.1:n.164+168C=
ENST00000579243.1:c.164+168C=	ENSP00000462568.1:n.164+168C=
ENST00000614341.4:c.164+168C=	ENSP00000480279.1:n.164+168C=
NM_001282489.2:c.-93+168C=	NP_001269418.1:n.-93+168C=
NM_173477.4:c.164+168C=	NP_775748.2:n.164+168C=
XM_011524296.1:c.-312C=	XP_011522598.1:n.-312C=
XM_011524296.2:c.-312C=	XP_011522598.1:n.-312C=
NM_173477.5:c.164+168C= MANE Select	NP_775748.2:n.164+168C=
NM_001282489.3:c.-93+168C=	NP_001269418.1:n.-93+168C=