Canonical Allele Identifier: CA2275256741

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74922739C= , CM000679.2:g.74922739C=	GRCh38
NC_000017.10:g.72918834C= , CM000679.1:g.72918834C=	GRCh37
NC_000017.9:g.70430429C=	NCBI36
NG_007882.1:g.5518G=
NG_033062.1:g.3465C=
NG_007882.2:g.5525G=
NG_033062.2:g.3465C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000614341.5:c.164+171G= MANE Select	ENSP00000480279.1:n.164+171G=
ENST00000579243.1:c.164+171G=	ENSP00000462568.1:n.164+171G=
ENST00000614341.4:c.164+171G=	ENSP00000480279.1:n.164+171G=
NM_001282489.2:c.-93+171G=	NP_001269418.1:n.-93+171G=
NM_173477.4:c.164+171G=	NP_775748.2:n.164+171G=
XM_011524296.1:c.-309G=	XP_011522598.1:n.-309G=
XM_011524296.2:c.-309G=	XP_011522598.1:n.-309G=
NM_173477.5:c.164+171G= MANE Select	NP_775748.2:n.164+171G=
NM_001282489.3:c.-93+171G=	NP_001269418.1:n.-93+171G=