Canonical Allele Identifier: CA656874910

Gene: USH1G

Linked Data

• COSMIC: COSN23399143

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.74916340_74916341insT , CM000679.2:g.74916340_74916341insT	GRCh38
NC_000017.10:g.72912432_72912433insT , CM000679.1:g.72912432_72912433insT	GRCh37
NC_000017.9:g.70424027_70424028insT	NCBI36
NG_007882.1:g.11919_11920insA
NG_007882.2:g.11923_11924insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000614341.5:c.*1732_*1733insA MANE Select	ENSP00000480279.1:n.*1732_*1733insA
ENST00000614341.4:c.*1732_*1733insA	ENSP00000480279.1:n.*1732_*1733insA
NM_001282489.2:c.*1732_*1733insA	NP_001269418.1:n.*1732_*1733insA
NM_173477.4:c.*1732_*1733insA	NP_775748.2:n.*1732_*1733insA
XM_011524296.1:c.*1732_*1733insA	XP_011522598.1:n.*1732_*1733insA
XM_011524296.2:c.*1732_*1733insA	XP_011522598.1:n.*1732_*1733insA
NM_173477.5:c.*1732_*1733insA MANE Select	NP_775748.2:n.*1732_*1733insA
NM_001282489.3:c.*1732_*1733insA	NP_001269418.1:n.*1732_*1733insA