Canonical Allele Identifier: CA293984107

Gene: USH1G

Linked Data

• ClinVar Variation Id: 808316
• ClinVar RCV Id: RCV000996605
• dbSNP Id: rs768235452
• gnomAD v2: 17-72916102-G-A
• gnomAD v4: 17-74920007-G-A
• MyVariant Identifiers: chr17:g.72916102G>A (hg19) ; chr17:g.74920007G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920007G>A , CM000679.2:g.74920007G>A	GRCh38
NC_000017.10:g.72916102G>A , CM000679.1:g.72916102G>A	GRCh37
NC_000017.9:g.70427697G>A	NCBI36
NG_007882.1:g.8250C>T
NG_033062.1:g.733G>A
NG_007882.2:g.8257C>T
NG_033062.2:g.733G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.829C>T MANE Select	ENSP00000480279.1:p.Leu277Phe
ENST00000579243.1:c.*428C>T	ENSP00000462568.1:n.*428C>T
ENST00000614341.4:c.829C>T	ENSP00000480279.1:p.Leu277Phe
NM_001282489.2:c.520C>T	NP_001269418.1:p.Leu174Phe
NM_173477.4:c.829C>T	NP_775748.2:p.Leu277Phe
XM_011524296.1:c.520C>T	XP_011522598.1:p.Leu174Phe
XM_011524296.2:c.520C>T	XP_011522598.1:p.Leu174Phe
NM_173477.5:c.829C>T MANE Select	NP_775748.2:p.Leu277Phe
NM_001282489.3:c.520C>T	NP_001269418.1:p.Leu174Phe