Canonical Allele Identifier: CA1184191016
Gene: GPR88 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539710_100539737delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT , CM000663.2:g.100539710_100539737delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT GRCh38
NC_000001.10:g.101005266_101005293delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT , CM000663.1:g.101005266_101005293delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT GRCh37
NC_000001.9:g.100777854_100777881delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT NCBI36
NG_053134.1:g.6539_6566delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.744_771delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT MANE Select ENSP00000314223.4:p.Pro248=
ENST00000315033.4:c.744_771delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT ENSP00000314223.4:p.Pro248=
NM_022049.2:c.744_771delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT NP_071332.2:p.Pro248=
NM_022049.3:c.744_771delinsGGGCGCCCAGCACGCGCCGGGCCCCGGT MANE Select NP_071332.2:p.Pro248=
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