Canonical Allele Identifier: CA502036398

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72916124T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920029T>C , CM000679.2:g.74920029T>C	GRCh38
NC_000017.10:g.72916124T>C , CM000679.1:g.72916124T>C	GRCh37
NC_000017.9:g.70427719T>C	NCBI36
NG_007882.1:g.8228A>G
NG_033062.1:g.755T>C
NG_007882.2:g.8235A>G
NG_033062.2:g.755T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.807A>G MANE Select	ENSP00000480279.1:p.Arg269=
ENST00000579243.1:c.*406A>G	ENSP00000462568.1:n.*406A>G
ENST00000614341.4:c.807A>G	ENSP00000480279.1:p.Arg269=
NM_001282489.2:c.498A>G	NP_001269418.1:p.Arg166=
NM_173477.4:c.807A>G	NP_775748.2:p.Arg269=
XM_011524296.1:c.498A>G	XP_011522598.1:p.Arg166=
XM_011524296.2:c.498A>G	XP_011522598.1:p.Arg166=
NM_173477.5:c.807A>G MANE Select	NP_775748.2:p.Arg269=
NM_001282489.3:c.498A>G	NP_001269418.1:p.Arg166=