Canonical Allele Identifier: CA400963043

Gene: USH1G

Linked Data

• ClinVar Variation Id: 2128462
• ClinVar RCV Id: RCV003036354
• dbSNP Id: rs1450585986
• gnomAD v2: 17-72916098-G-A
• gnomAD v3: 17-74920003-G-A
• gnomAD v4: 17-74920003-G-A
• MyVariant Identifiers: chr17:g.72916098G>A (hg19) ; chr17:g.74920003G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920003G>A , CM000679.2:g.74920003G>A	GRCh38
NC_000017.10:g.72916098G>A , CM000679.1:g.72916098G>A	GRCh37
NC_000017.9:g.70427693G>A	NCBI36
NG_007882.1:g.8254C>T
NG_033062.1:g.729G>A
NG_007882.2:g.8261C>T
NG_033062.2:g.729G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.833C>T MANE Select	ENSP00000480279.1:p.Ser278Leu
ENST00000579243.1:c.*432C>T	ENSP00000462568.1:n.*432C>T
ENST00000614341.4:c.833C>T	ENSP00000480279.1:p.Ser278Leu
NM_001282489.2:c.524C>T	NP_001269418.1:p.Ser175Leu
NM_173477.4:c.833C>T	NP_775748.2:p.Ser278Leu
XM_011524296.1:c.524C>T	XP_011522598.1:p.Ser175Leu
XM_011524296.2:c.524C>T	XP_011522598.1:p.Ser175Leu
NM_173477.5:c.833C>T MANE Select	NP_775748.2:p.Ser278Leu
NM_001282489.3:c.524C>T	NP_001269418.1:p.Ser175Leu