Canonical Allele Identifier: CA2646776780
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539598del , CM000663.2:g.100539598del GRCh38
NC_000001.10:g.101005154del , CM000663.1:g.101005154del GRCh37
NC_000001.9:g.100777742del NCBI36
NG_053134.1:g.6427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.632del MANE Select ENSP00000314223.4:p.Cys211SerfsTer?
ENST00000315033.4:c.632del ENSP00000314223.4:p.Cys211SerfsTer?
NM_022049.2:c.632del NP_071332.2:p.Cys211SerfsTer?
NM_022049.3:c.632del MANE Select NP_071332.2:p.Cys211SerfsTer?