Canonical Allele Identifier: CA2646776673

Gene: GPR88

Linked Data

• gnomAD v4: 1-100539556-CCGCCGCGGCGCTGCTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539560_100539576del , CM000663.2:g.100539560_100539576del	GRCh38
NC_000001.10:g.101005116_101005132del , CM000663.1:g.101005116_101005132del	GRCh37
NC_000001.9:g.100777704_100777720del	NCBI36
NG_053134.1:g.6389_6405del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.594_610del MANE Select	ENSP00000314223.4:p.Ala199AspfsTer?
ENST00000315033.4:c.594_610del	ENSP00000314223.4:p.Ala199AspfsTer?
NM_022049.2:c.594_610del	NP_071332.2:p.Ala199AspfsTer?
NM_022049.3:c.594_610del MANE Select	NP_071332.2:p.Ala199AspfsTer?