Canonical Allele Identifier: CA2646776731
Gene: GPR88 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539578_100539579del , CM000663.2:g.100539578_100539579del GRCh38
NC_000001.10:g.101005134_101005135del , CM000663.1:g.101005134_101005135del GRCh37
NC_000001.9:g.100777722_100777723del NCBI36
NG_053134.1:g.6407_6408del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.612_613del MANE Select ENSP00000314223.4:p.Gln204HisfsTer?
ENST00000315033.4:c.612_613del ENSP00000314223.4:p.Gln204HisfsTer?
NM_022049.2:c.612_613del NP_071332.2:p.Gln204HisfsTer?
NM_022049.3:c.612_613del MANE Select NP_071332.2:p.Gln204HisfsTer?