Canonical Allele Identifier: CA8753914

Gene: USH1G

Linked Data

• ClinVar Variation Id: 1107751
• ClinVar RCV Id: RCV001432998
• dbSNP Id: rs755013643
• ExAC: 17:72915725 C / T
• gnomAD v2: 17-72915725-C-T
• gnomAD v3: 17-74919630-C-T
• gnomAD v4: 17-74919630-C-T
• MyVariant Identifiers: chr17:g.72915725C>T (hg19) ; chr17:g.74919630C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919630C>T , CM000679.2:g.74919630C>T	GRCh38
NC_000017.10:g.72915725C>T , CM000679.1:g.72915725C>T	GRCh37
NC_000017.9:g.70427320C>T	NCBI36
NG_007882.1:g.8627G>A
NG_033062.1:g.356C>T
NG_007882.2:g.8634G>A
NG_033062.2:g.356C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1206G>A MANE Select	ENSP00000480279.1:p.Glu402=
ENST00000579243.1:c.*805G>A	ENSP00000462568.1:n.*805G>A
ENST00000614341.4:c.1206G>A	ENSP00000480279.1:p.Glu402=
NM_001282489.2:c.897G>A	NP_001269418.1:p.Glu299=
NM_173477.4:c.1206G>A	NP_775748.2:p.Glu402=
XM_011524296.1:c.897G>A	XP_011522598.1:p.Glu299=
XM_011524296.2:c.897G>A	XP_011522598.1:p.Glu299=
NM_173477.5:c.1206G>A MANE Select	NP_775748.2:p.Glu402=
NM_001282489.3:c.897G>A	NP_001269418.1:p.Glu299=