Canonical Allele Identifier: CA2646776886
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539647-C-CGCT
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539648_100539649insCTG , CM000663.2:g.100539648_100539649insCTG GRCh38
NC_000001.10:g.101005204_101005205insCTG , CM000663.1:g.101005204_101005205insCTG GRCh37
NC_000001.9:g.100777792_100777793insCTG NCBI36
NG_053134.1:g.6477_6478insCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.682_683insCTG MANE Select ENSP00000314223.4:p.Ser227_Val228insAla
ENST00000315033.4:c.682_683insCTG ENSP00000314223.4:p.Ser227_Val228insAla
NM_022049.2:c.682_683insCTG NP_071332.2:p.Ser227_Val228insAla
NM_022049.3:c.682_683insCTG MANE Select NP_071332.2:p.Ser227_Val228insAla
Search 100 bp 5'
Search 100 bp 3'