Canonical Allele Identifier: CA2646776851
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539626-TGTCAGCGTCAAGCGG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539635_100539649del , CM000663.2:g.100539635_100539649del GRCh38
NC_000001.10:g.101005191_101005205del , CM000663.1:g.101005191_101005205del GRCh37
NC_000001.9:g.100777779_100777793del NCBI36
NG_053134.1:g.6464_6478del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.669_683del MANE Select ENSP00000314223.4:p.Lys224_Val228del
ENST00000315033.4:c.669_683del ENSP00000314223.4:p.Lys224_Val228del
NM_022049.2:c.669_683del NP_071332.2:p.Lys224_Val228del
NM_022049.3:c.669_683del MANE Select NP_071332.2:p.Lys224_Val228del
Search 100 bp 5'
Search 100 bp 3'