Canonical Allele Identifier: CA1184190791
Gene: GPR88 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539543_100539561delinsCCGGCGCTGCTGGCCGCCG , CM000663.2:g.100539543_100539561delinsCCGGCGCTGCTGGCCGCCG GRCh38
NC_000001.10:g.101005099_101005117delinsCCGGCGCTGCTGGCCGCCG , CM000663.1:g.101005099_101005117delinsCCGGCGCTGCTGGCCGCCG GRCh37
NC_000001.9:g.100777687_100777705delinsCCGGCGCTGCTGGCCGCCG NCBI36
NG_053134.1:g.6372_6390delinsCCGGCGCTGCTGGCCGCCG

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.577_595delinsCCGGCGCTGCTGGCCGCCG MANE Select ENSP00000314223.4:p.Pro193=
ENST00000315033.4:c.577_595delinsCCGGCGCTGCTGGCCGCCG ENSP00000314223.4:p.Pro193=
NM_022049.2:c.577_595delinsCCGGCGCTGCTGGCCGCCG NP_071332.2:p.Pro193=
NM_022049.3:c.577_595delinsCCGGCGCTGCTGGCCGCCG MANE Select NP_071332.2:p.Pro193=
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