Canonical Allele Identifier: CA2275255175

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919616A= , CM000679.2:g.74919616A=	GRCh38
NC_000017.10:g.72915711A= , CM000679.1:g.72915711A=	GRCh37
NC_000017.9:g.70427306A=	NCBI36
NG_007882.1:g.8641T=
NG_033062.1:g.342A=
NG_007882.2:g.8648T=
NG_033062.2:g.342A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1220T= MANE Select	ENSP00000480279.1:p.Leu407=
ENST00000579243.1:c.*819T=	ENSP00000462568.1:n.*819T=
ENST00000614341.4:c.1220T=	ENSP00000480279.1:p.Leu407=
NM_001282489.2:c.911T=	NP_001269418.1:p.Leu304=
NM_173477.4:c.1220T=	NP_775748.2:p.Leu407=
XM_011524296.1:c.911T=	XP_011522598.1:p.Leu304=
XM_011524296.2:c.911T=	XP_011522598.1:p.Leu304=
NM_173477.5:c.1220T= MANE Select	NP_775748.2:p.Leu407=
NM_001282489.3:c.911T=	NP_001269418.1:p.Leu304=