Canonical Allele Identifier: CA2275255440

Gene: USH1G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920109A= , CM000679.2:g.74920109A=	GRCh38
NC_000017.10:g.72916204A= , CM000679.1:g.72916204A=	GRCh37
NC_000017.9:g.70427799A=	NCBI36
NG_007882.1:g.8148T=
NG_033062.1:g.835A=
NG_007882.2:g.8155T=
NG_033062.2:g.835A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.727T= MANE Select	ENSP00000480279.1:p.Ser243=
ENST00000579243.1:c.*326T=	ENSP00000462568.1:n.*326T=
ENST00000614341.4:c.727T=	ENSP00000480279.1:p.Ser243=
NM_001282489.2:c.418T=	NP_001269418.1:p.Ser140=
NM_173477.4:c.727T=	NP_775748.2:p.Ser243=
XM_011524296.1:c.418T=	XP_011522598.1:p.Ser140=
XM_011524296.2:c.418T=	XP_011522598.1:p.Ser140=
NM_173477.5:c.727T= MANE Select	NP_775748.2:p.Ser243=
NM_001282489.3:c.418T=	NP_001269418.1:p.Ser140=