Canonical Allele Identifier: CA2646776923
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539978-TG-T
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539980del , CM000663.2:g.100539980del GRCh38
NC_000001.10:g.101005536del , CM000663.1:g.101005536del GRCh37
NC_000001.9:g.100778124del NCBI36
NG_053134.1:g.6809del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1014del MANE Select ENSP00000314223.4:p.Trp338Ter
ENST00000315033.4:c.1014del ENSP00000314223.4:p.Trp338Ter
NM_022049.2:c.1014del NP_071332.2:p.Trp338Ter
NM_022049.3:c.1014del MANE Select NP_071332.2:p.Trp338Ter
Search 100 bp 5'
Search 100 bp 3'