Canonical Allele Identifier: CA2646776897
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539687-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539689del , CM000663.2:g.100539689del GRCh38
NC_000001.10:g.101005245del , CM000663.1:g.101005245del GRCh37
NC_000001.9:g.100777833del NCBI36
NG_053134.1:g.6518del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.723del MANE Select ENSP00000314223.4:p.Ala242ProfsTer?
ENST00000315033.4:c.723del ENSP00000314223.4:p.Ala242ProfsTer?
NM_022049.2:c.723del NP_071332.2:p.Ala242ProfsTer?
NM_022049.3:c.723del MANE Select NP_071332.2:p.Ala242ProfsTer?
Search 100 bp 5'
Search 100 bp 3'