Canonical Allele Identifier: CA2646776889

Gene: GPR88

Linked Data

• gnomAD v4: 1-100539664-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539665del , CM000663.2:g.100539665del	GRCh38
NC_000001.10:g.101005221del , CM000663.1:g.101005221del	GRCh37
NC_000001.9:g.100777809del	NCBI36
NG_053134.1:g.6494del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.699del MANE Select	ENSP00000314223.4:p.Leu234CysfsTer?
ENST00000315033.4:c.699del	ENSP00000314223.4:p.Leu234CysfsTer?
NM_022049.2:c.699del	NP_071332.2:p.Leu234CysfsTer?
NM_022049.3:c.699del MANE Select	NP_071332.2:p.Leu234CysfsTer?