Canonical Allele Identifier: CA2646776900
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539694-CCG-C
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539696_100539697del , CM000663.2:g.100539696_100539697del GRCh38
NC_000001.10:g.101005252_101005253del , CM000663.1:g.101005252_101005253del GRCh37
NC_000001.9:g.100777840_100777841del NCBI36
NG_053134.1:g.6525_6526del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.730_731del MANE Select ENSP00000314223.4:p.Ala244ArgfsTer?
ENST00000315033.4:c.730_731del ENSP00000314223.4:p.Ala244ArgfsTer?
NM_022049.2:c.730_731del NP_071332.2:p.Ala244ArgfsTer?
NM_022049.3:c.730_731del MANE Select NP_071332.2:p.Ala244ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'