Canonical Allele Identifier: CA971118
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs771443704
ExAC: 1:101005241 G / GCGCCGC
gnomAD v2: 1-101005241-G-GCGCCGC
gnomAD v4: 1-100539685-G-GCGCCGC
MyVariant Identifiers: chr1:g.101005244_101005245insCGCCGC (hg19) chr1:g.101005241_101005242insCGCCGC (hg19) chr1:g.100539688_100539689insCGCCGC (hg38) chr1:g.100539685_100539686insCGCCGC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539699_100539704dup , CM000663.2:g.100539699_100539704dup GRCh38
NC_000001.10:g.101005255_101005260dup , CM000663.1:g.101005255_101005260dup GRCh37
NC_000001.9:g.100777843_100777848dup NCBI36
NG_053134.1:g.6528_6533dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.733_738dup MANE Select ENSP00000314223.4:p.Ala246_Phe247insAlaAla
ENST00000315033.4:c.733_738dup ENSP00000314223.4:p.Ala246_Phe247insAlaAla
NM_022049.2:c.733_738dup NP_071332.2:p.Ala246_Phe247insAlaAla
NM_022049.3:c.733_738dup MANE Select NP_071332.2:p.Ala246_Phe247insAlaAla
Search 100 bp 5'
Search 100 bp 3'