Canonical Allele Identifier: CA2646776914

Gene: GPR88

Linked Data

• gnomAD v4: 1-100539742-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539746_100539747del , CM000663.2:g.100539746_100539747del	GRCh38
NC_000001.10:g.101005302_101005303del , CM000663.1:g.101005302_101005303del	GRCh37
NC_000001.9:g.100777890_100777891del	NCBI36
NG_053134.1:g.6575_6576del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.780_781del MANE Select	ENSP00000314223.4:p.His261ProfsTer?
ENST00000315033.4:c.780_781del	ENSP00000314223.4:p.His261ProfsTer?
NM_022049.2:c.780_781del	NP_071332.2:p.His261ProfsTer?
NM_022049.3:c.780_781del MANE Select	NP_071332.2:p.His261ProfsTer?