Canonical Allele Identifier: CA400964238

Gene: USH1G

Linked Data

• gnomAD v4: 17-74920201-C-A
• MyVariant Identifiers: chr17:g.72916296C>A (hg19) ; chr17:g.74920201C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920201C>A , CM000679.2:g.74920201C>A	GRCh38
NC_000017.10:g.72916296C>A , CM000679.1:g.72916296C>A	GRCh37
NC_000017.9:g.70427891C>A	NCBI36
NG_007882.1:g.8056G>T
NG_033062.1:g.927C>A
NG_007882.2:g.8063G>T
NG_033062.2:g.927C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.635G>T MANE Select	ENSP00000480279.1:p.Gly212Val
ENST00000579243.1:c.*234G>T	ENSP00000462568.1:n.*234G>T
ENST00000614341.4:c.635G>T	ENSP00000480279.1:p.Gly212Val
NM_001282489.2:c.326G>T	NP_001269418.1:p.Gly109Val
NM_173477.4:c.635G>T	NP_775748.2:p.Gly212Val
XM_011524296.1:c.326G>T	XP_011522598.1:p.Gly109Val
XM_011524296.2:c.326G>T	XP_011522598.1:p.Gly109Val
NM_173477.5:c.635G>T MANE Select	NP_775748.2:p.Gly212Val
NM_001282489.3:c.326G>T	NP_001269418.1:p.Gly109Val