Canonical Allele Identifier: CA971106
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs745394911
ExAC: 1:101005099 CCGGCGCTGCTGGCCGCCG / C
gnomAD v2: 1-101005099-CCGGCGCTGCTGGCCGCCG-C
gnomAD v3: 1-100539543-CCGGCGCTGCTGGCCGCCG-C
gnomAD v4: 1-100539543-CCGGCGCTGCTGGCCGCCG-C
MyVariant Identifiers: chr1:g.101005100_101005117del (hg19) chr1:g.100539544_100539561del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539557_100539574del , CM000663.2:g.100539557_100539574del GRCh38
NC_000001.10:g.101005113_101005130del , CM000663.1:g.101005113_101005130del GRCh37
NC_000001.9:g.100777701_100777718del NCBI36
NG_053134.1:g.6386_6403del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.591_608del MANE Select ENSP00000314223.4:p.Ala198_Ala203del
ENST00000315033.4:c.591_608del ENSP00000314223.4:p.Ala198_Ala203del
NM_022049.2:c.591_608del NP_071332.2:p.Ala198_Ala203del
NM_022049.3:c.591_608del MANE Select NP_071332.2:p.Ala198_Ala203del
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