Canonical Allele Identifier: CA627376760
Gene: USH1G HGNC NCBI

Linked Data

dbSNP Id: rs1404630568

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.74922843del , CM000679.2:g.74922843del GRCh38
NC_000017.10:g.72918938del , CM000679.1:g.72918938del GRCh37
NC_000017.9:g.70430533del NCBI36
NG_007882.1:g.5415del
NG_033062.1:g.3569del
NG_007882.2:g.5422del
NG_033062.2:g.3569del

Transcript Alleles

HGVS Amino-acid change
ENST00000614341.5:c.164+68del MANE Select ENSP00000480279.1:n.164+68del
ENST00000579243.1:c.164+68del ENSP00000462568.1:n.164+68del
ENST00000614341.4:c.164+68del ENSP00000480279.1:n.164+68del
NM_001282489.2:c.-93+68del NP_001269418.1:n.-93+68del
NM_173477.4:c.164+68del NP_775748.2:n.164+68del
XM_011524296.1:c.-412del XP_011522598.1:n.-412del
XM_011524296.2:c.-412del XP_011522598.1:n.-412del
NM_173477.5:c.164+68del MANE Select NP_775748.2:n.164+68del
NM_001282489.3:c.-93+68del NP_001269418.1:n.-93+68del