Canonical Allele Identifier: CA2639739533

Gene: USH1G

Linked Data

• gnomAD v4: 17-74916368-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74916368C>A , CM000679.2:g.74916368C>A	GRCh38
NC_000017.10:g.72912460C>A , CM000679.1:g.72912460C>A	GRCh37
NC_000017.9:g.70424055C>A	NCBI36
NG_007882.1:g.11892G>T
NG_007882.2:g.11896G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.*1705G>T MANE Select	ENSP00000480279.1:n.*1705G>T
ENST00000614341.4:c.*1705G>T	ENSP00000480279.1:n.*1705G>T
NM_001282489.2:c.*1705G>T	NP_001269418.1:n.*1705G>T
NM_173477.4:c.*1705G>T	NP_775748.2:n.*1705G>T
XM_011524296.1:c.*1705G>T	XP_011522598.1:n.*1705G>T
XM_011524296.2:c.*1705G>T	XP_011522598.1:n.*1705G>T
NM_173477.5:c.*1705G>T MANE Select	NP_775748.2:n.*1705G>T
NM_001282489.3:c.*1705G>T	NP_001269418.1:n.*1705G>T