Canonical Allele Identifier: CA502036420

Gene: USH1G

Linked Data

• dbSNP Id: rs2038906954
• gnomAD v4: 17-74919561-G-A
• MyVariant Identifiers: chr17:g.72915656G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919561G>A , CM000679.2:g.74919561G>A	GRCh38
NC_000017.10:g.72915656G>A , CM000679.1:g.72915656G>A	GRCh37
NC_000017.9:g.70427251G>A	NCBI36
NG_007882.1:g.8696C>T
NG_033062.1:g.287G>A
NG_007882.2:g.8703C>T
NG_033062.2:g.287G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1275C>T MANE Select	ENSP00000480279.1:p.Asp425=
ENST00000579243.1:c.*874C>T	ENSP00000462568.1:n.*874C>T
ENST00000614341.4:c.1275C>T	ENSP00000480279.1:p.Asp425=
NM_001282489.2:c.966C>T	NP_001269418.1:p.Asp322=
NM_173477.4:c.1275C>T	NP_775748.2:p.Asp425=
XM_011524296.1:c.966C>T	XP_011522598.1:p.Asp322=
XM_011524296.2:c.966C>T	XP_011522598.1:p.Asp322=
NM_173477.5:c.1275C>T MANE Select	NP_775748.2:p.Asp425=
NM_001282489.3:c.966C>T	NP_001269418.1:p.Asp322=