Canonical Allele Identifier: CA2646776901
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539704_100539705insGCCCCGCC , CM000663.2:g.100539704_100539705insGCCCCGCC GRCh38
NC_000001.10:g.101005260_101005261insGCCCCGCC , CM000663.1:g.101005260_101005261insGCCCCGCC GRCh37
NC_000001.9:g.100777848_100777849insGCCCCGCC NCBI36
NG_053134.1:g.6533_6534insGCCCCGCC

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.738_739insGCCCCGCC MANE Select ENSP00000314223.4:p.Phe247AlafsTer?
ENST00000315033.4:c.738_739insGCCCCGCC ENSP00000314223.4:p.Phe247AlafsTer?
NM_022049.2:c.738_739insGCCCCGCC NP_071332.2:p.Phe247AlafsTer?
NM_022049.3:c.738_739insGCCCCGCC MANE Select NP_071332.2:p.Phe247AlafsTer?