Canonical Allele Identifier: CA2646776898
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539693del , CM000663.2:g.100539693del GRCh38
NC_000001.10:g.101005249del , CM000663.1:g.101005249del GRCh37
NC_000001.9:g.100777837del NCBI36
NG_053134.1:g.6522del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.727del MANE Select ENSP00000314223.4:p.Ala243ProfsTer?
ENST00000315033.4:c.727del ENSP00000314223.4:p.Ala243ProfsTer?
NM_022049.2:c.727del NP_071332.2:p.Ala243ProfsTer?
NM_022049.3:c.727del MANE Select NP_071332.2:p.Ala243ProfsTer?