Canonical Allele Identifier: CA2646776906
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539707-C-CAGA
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539707_100539708insAGA , CM000663.2:g.100539707_100539708insAGA GRCh38
NC_000001.10:g.101005263_101005264insAGA , CM000663.1:g.101005263_101005264insAGA GRCh37
NC_000001.9:g.100777851_100777852insAGA NCBI36
NG_053134.1:g.6536_6537insAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.741_742insAGA MANE Select ENSP00000314223.4:p.Phe247_Pro248insArg
ENST00000315033.4:c.741_742insAGA ENSP00000314223.4:p.Phe247_Pro248insArg
NM_022049.2:c.741_742insAGA NP_071332.2:p.Phe247_Pro248insArg
NM_022049.3:c.741_742insAGA MANE Select NP_071332.2:p.Phe247_Pro248insArg
Search 100 bp 5'
Search 100 bp 3'