Canonical Allele Identifier: CA400961429

Gene: USH1G

Linked Data

• ClinVar Variation Id: 929926
• ClinVar RCV Id: RCV001195266
• dbSNP Id: rs1282068985
• gnomAD v2: 17-72915714-G-C
• gnomAD v4: 17-74919619-G-C
• MyVariant Identifiers: chr17:g.72915714G>C (hg19) ; chr17:g.74919619G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919619G>C , CM000679.2:g.74919619G>C	GRCh38
NC_000017.10:g.72915714G>C , CM000679.1:g.72915714G>C	GRCh37
NC_000017.9:g.70427309G>C	NCBI36
NG_007882.1:g.8638C>G
NG_033062.1:g.345G>C
NG_007882.2:g.8645C>G
NG_033062.2:g.345G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1217C>G MANE Select	ENSP00000480279.1:p.Ala406Gly
ENST00000579243.1:c.*816C>G	ENSP00000462568.1:n.*816C>G
ENST00000614341.4:c.1217C>G	ENSP00000480279.1:p.Ala406Gly
NM_001282489.2:c.908C>G	NP_001269418.1:p.Ala303Gly
NM_173477.4:c.1217C>G	NP_775748.2:p.Ala406Gly
XM_011524296.1:c.908C>G	XP_011522598.1:p.Ala303Gly
XM_011524296.2:c.908C>G	XP_011522598.1:p.Ala303Gly
NM_173477.5:c.1217C>G MANE Select	NP_775748.2:p.Ala406Gly
NM_001282489.3:c.908C>G	NP_001269418.1:p.Ala303Gly