Canonical Allele Identifier: CA2639739179

Gene: USH1G

Linked Data

• gnomAD v4: 17-74916248-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74916252del , CM000679.2:g.74916252del	GRCh38
NC_000017.10:g.72912344del , CM000679.1:g.72912344del	GRCh37
NC_000017.9:g.70423939del	NCBI36
NG_007882.1:g.12011del
NG_007882.2:g.12015del

Transcript Alleles

HGVS	Amino-acid change
ENST00000614341.5:c.*1824del MANE Select	ENSP00000480279.1:n.*1824del
ENST00000614341.4:c.*1824del	ENSP00000480279.1:n.*1824del
NM_001282489.2:c.*1824del	NP_001269418.1:n.*1824del
NM_173477.4:c.*1824del	NP_775748.2:n.*1824del
XM_011524296.1:c.*1824del	XP_011522598.1:n.*1824del
XM_011524296.2:c.*1824del	XP_011522598.1:n.*1824del
NM_173477.5:c.*1824del MANE Select	NP_775748.2:n.*1824del
NM_001282489.3:c.*1824del	NP_001269418.1:n.*1824del