Canonical Allele Identifier: CA2646776913

Gene: GPR88

Linked Data

• gnomAD v4: 1-100539734-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539736dup , CM000663.2:g.100539736dup	GRCh38
NC_000001.10:g.101005292dup , CM000663.1:g.101005292dup	GRCh37
NC_000001.9:g.100777880dup	NCBI36
NG_053134.1:g.6565dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.770dup MANE Select	ENSP00000314223.4:p.Gly258TrpfsTer?
ENST00000315033.4:c.770dup	ENSP00000314223.4:p.Gly258TrpfsTer?
NM_022049.2:c.770dup	NP_071332.2:p.Gly258TrpfsTer?
NM_022049.3:c.770dup MANE Select	NP_071332.2:p.Gly258TrpfsTer?