Canonical Allele Identifier: CA400963353

Gene: USH1G

Linked Data

• MyVariant Identifiers: chr17:g.72916150A>G (hg19) ; chr17:g.74920055A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920055A>G , CM000679.2:g.74920055A>G	GRCh38
NC_000017.10:g.72916150A>G , CM000679.1:g.72916150A>G	GRCh37
NC_000017.9:g.70427745A>G	NCBI36
NG_007882.1:g.8202T>C
NG_033062.1:g.781A>G
NG_007882.2:g.8209T>C
NG_033062.2:g.781A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.781T>C MANE Select	ENSP00000480279.1:p.Tyr261His
ENST00000579243.1:c.*380T>C	ENSP00000462568.1:n.*380T>C
ENST00000614341.4:c.781T>C	ENSP00000480279.1:p.Tyr261His
NM_001282489.2:c.472T>C	NP_001269418.1:p.Tyr158His
NM_173477.4:c.781T>C	NP_775748.2:p.Tyr261His
XM_011524296.1:c.472T>C	XP_011522598.1:p.Tyr158His
XM_011524296.2:c.472T>C	XP_011522598.1:p.Tyr158His
NM_173477.5:c.781T>C MANE Select	NP_775748.2:p.Tyr261His
NM_001282489.3:c.472T>C	NP_001269418.1:p.Tyr158His