Canonical Allele Identifier: CA8753995

Gene: USH1G

Linked Data

• dbSNP Id: rs751974726
• ExAC: 17:72916118 C / A
• gnomAD v2: 17-72916118-C-A
• gnomAD v3: 17-74920023-C-A
• gnomAD v4: 17-74920023-C-A
• MyVariant Identifiers: chr17:g.72916118C>A (hg19) ; chr17:g.74920023C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74920023C>A , CM000679.2:g.74920023C>A	GRCh38
NC_000017.10:g.72916118C>A , CM000679.1:g.72916118C>A	GRCh37
NC_000017.9:g.70427713C>A	NCBI36
NG_007882.1:g.8234G>T
NG_033062.1:g.749C>A
NG_007882.2:g.8241G>T
NG_033062.2:g.749C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.813G>T MANE Select	ENSP00000480279.1:p.Pro271=
ENST00000579243.1:c.*412G>T	ENSP00000462568.1:n.*412G>T
ENST00000614341.4:c.813G>T	ENSP00000480279.1:p.Pro271=
NM_001282489.2:c.504G>T	NP_001269418.1:p.Pro168=
NM_173477.4:c.813G>T	NP_775748.2:p.Pro271=
XM_011524296.1:c.504G>T	XP_011522598.1:p.Pro168=
XM_011524296.2:c.504G>T	XP_011522598.1:p.Pro168=
NM_173477.5:c.813G>T MANE Select	NP_775748.2:p.Pro271=
NM_001282489.3:c.504G>T	NP_001269418.1:p.Pro168=