Canonical Allele Identifier: CA2639743411

Gene: USH1G

Linked Data

• gnomAD v4: 17-74917206-TGCCTGTCCCAG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74917212_74917222del , CM000679.2:g.74917212_74917222del	GRCh38
NC_000017.10:g.72913306_72913316del , CM000679.1:g.72913306_72913316del	GRCh37
NC_000017.9:g.70424901_70424911del	NCBI36
NG_007882.1:g.11041_11051del
NG_007882.2:g.11047_11057del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.*856_*866del MANE Select	ENSP00000480279.1:n.*856_*866del
ENST00000614341.4:c.*856_*866del	ENSP00000480279.1:n.*856_*866del
NM_001282489.2:c.*856_*866del	NP_001269418.1:n.*856_*866del
NM_173477.4:c.*856_*866del	NP_775748.2:n.*856_*866del
XM_011524296.1:c.*856_*866del	XP_011522598.1:n.*856_*866del
XM_011524296.2:c.*856_*866del	XP_011522598.1:n.*856_*866del
NM_173477.5:c.*856_*866del MANE Select	NP_775748.2:n.*856_*866del
NM_001282489.3:c.*856_*866del	NP_001269418.1:n.*856_*866del