Canonical Allele Identifier: CA502036393

Gene: USH1G

Linked Data

• gnomAD v4: 17-74919540-T-G
• MyVariant Identifiers: chr17:g.72915635T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74919540T>G , CM000679.2:g.74919540T>G	GRCh38
NC_000017.10:g.72915635T>G , CM000679.1:g.72915635T>G	GRCh37
NC_000017.9:g.70427230T>G	NCBI36
NG_007882.1:g.8717A>C
NG_033062.1:g.266T>G
NG_007882.2:g.8724A>C
NG_033062.2:g.266T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.1296A>C MANE Select	ENSP00000480279.1:p.Pro432=
ENST00000579243.1:c.*895A>C	ENSP00000462568.1:n.*895A>C
ENST00000614341.4:c.1296A>C	ENSP00000480279.1:p.Pro432=
NM_001282489.2:c.987A>C	NP_001269418.1:p.Pro329=
NM_173477.4:c.1296A>C	NP_775748.2:p.Pro432=
XM_011524296.1:c.987A>C	XP_011522598.1:p.Pro329=
XM_011524296.2:c.987A>C	XP_011522598.1:p.Pro329=
NM_173477.5:c.1296A>C MANE Select	NP_775748.2:p.Pro432=
NM_001282489.3:c.987A>C	NP_001269418.1:p.Pro329=