Canonical Allele Identifier: CA2646776801
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539607del , CM000663.2:g.100539607del GRCh38
NC_000001.10:g.101005163del , CM000663.1:g.101005163del GRCh37
NC_000001.9:g.100777751del NCBI36
NG_053134.1:g.6436del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.641del MANE Select ENSP00000314223.4:p.Gly214AlafsTer?
ENST00000315033.4:c.641del ENSP00000314223.4:p.Gly214AlafsTer?
NM_022049.2:c.641del NP_071332.2:p.Gly214AlafsTer?
NM_022049.3:c.641del MANE Select NP_071332.2:p.Gly214AlafsTer?