Canonical Allele Identifier: CA2646776642
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539514_100539565del , CM000663.2:g.100539514_100539565del GRCh38
NC_000001.10:g.101005070_101005121del , CM000663.1:g.101005070_101005121del GRCh37
NC_000001.9:g.100777658_100777709del NCBI36
NG_053134.1:g.6343_6394del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.548_599del MANE Select ENSP00000314223.4:p.Pro183ArgfsTer?
ENST00000315033.4:c.548_599del ENSP00000314223.4:p.Pro183ArgfsTer?
NM_022049.2:c.548_599del NP_071332.2:p.Pro183ArgfsTer?
NM_022049.3:c.548_599del MANE Select NP_071332.2:p.Pro183ArgfsTer?