Canonical Allele Identifier: CA2646776895
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539685_100539686insGGC , CM000663.2:g.100539685_100539686insGGC GRCh38
NC_000001.10:g.101005241_101005242insGGC , CM000663.1:g.101005241_101005242insGGC GRCh37
NC_000001.9:g.100777829_100777830insGGC NCBI36
NG_053134.1:g.6514_6515insGGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.719_720insGGC MANE Select ENSP00000314223.4:p.Cys240delinsTrpAla
ENST00000315033.4:c.719_720insGGC ENSP00000314223.4:p.Cys240delinsTrpAla
NM_022049.2:c.719_720insGGC NP_071332.2:p.Cys240delinsTrpAla
NM_022049.3:c.719_720insGGC MANE Select NP_071332.2:p.Cys240delinsTrpAla