Canonical Allele Identifier: CA656874933

Gene: USH1G

Linked Data

• COSMIC: COSN19298180

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74917343_74917344insA , CM000679.2:g.74917343_74917344insA	GRCh38
NC_000017.10:g.72913437_72913438insA , CM000679.1:g.72913437_72913438insA	GRCh37
NC_000017.9:g.70425032_70425033insA	NCBI36
NG_007882.1:g.10914_10915insT
NG_007882.2:g.10920_10921insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.*729_*730insT MANE Select	ENSP00000480279.1:n.*729_*730insT
ENST00000614341.4:c.*729_*730insT	ENSP00000480279.1:n.*729_*730insT
NM_001282489.2:c.*729_*730insT	NP_001269418.1:n.*729_*730insT
NM_173477.4:c.*729_*730insT	NP_775748.2:n.*729_*730insT
XM_011524296.1:c.*729_*730insT	XP_011522598.1:n.*729_*730insT
XM_011524296.2:c.*729_*730insT	XP_011522598.1:n.*729_*730insT
NM_173477.5:c.*729_*730insT MANE Select	NP_775748.2:n.*729_*730insT
NM_001282489.3:c.*729_*730insT	NP_001269418.1:n.*729_*730insT