Canonical Allele Identifier: CA2275256747

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74922750T= , CM000679.2:g.74922750T=	GRCh38
NC_000017.10:g.72918845T= , CM000679.1:g.72918845T=	GRCh37
NC_000017.9:g.70430440T=	NCBI36
NG_007882.1:g.5507A=
NG_033062.1:g.3476T=
NG_007882.2:g.5514A=
NG_033062.2:g.3476T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.164+160A= MANE Select	ENSP00000480279.1:n.164+160A=
ENST00000579243.1:c.164+160A=	ENSP00000462568.1:n.164+160A=
ENST00000614341.4:c.164+160A=	ENSP00000480279.1:n.164+160A=
NM_001282489.2:c.-93+160A=	NP_001269418.1:n.-93+160A=
NM_173477.4:c.164+160A=	NP_775748.2:n.164+160A=
XM_011524296.1:c.-320A=	XP_011522598.1:n.-320A=
XM_011524296.2:c.-320A=	XP_011522598.1:n.-320A=
NM_173477.5:c.164+160A= MANE Select	NP_775748.2:n.164+160A=
NM_001282489.3:c.-93+160A=	NP_001269418.1:n.-93+160A=