Canonical Allele Identifier: CA2646776887

Gene: GPR88

Linked Data

• gnomAD v4: 1-100539656-CT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.100539658del , CM000663.2:g.100539658del	GRCh38
NC_000001.10:g.101005214del , CM000663.1:g.101005214del	GRCh37
NC_000001.9:g.100777802del	NCBI36
NG_053134.1:g.6487del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315033.5:c.692del MANE Select	ENSP00000314223.4:p.Phe231SerfsTer?
ENST00000315033.4:c.692del	ENSP00000314223.4:p.Phe231SerfsTer?
NM_022049.2:c.692del	NP_071332.2:p.Phe231SerfsTer?
NM_022049.3:c.692del MANE Select	NP_071332.2:p.Phe231SerfsTer?