Canonical Allele Identifier: CA2646776925
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100540024-GCGTCGGCGACGCGGCGGC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540027_100540044del , CM000663.2:g.100540027_100540044del GRCh38
NC_000001.10:g.101005583_101005600del , CM000663.1:g.101005583_101005600del GRCh37
NC_000001.9:g.100778171_100778188del NCBI36
NG_053134.1:g.6856_6873del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1061_1078del MANE Select ENSP00000314223.4:p.Val354_Ala359del
ENST00000315033.4:c.1061_1078del ENSP00000314223.4:p.Val354_Ala359del
NM_022049.2:c.1061_1078del NP_071332.2:p.Val354_Ala359del
NM_022049.3:c.1061_1078del MANE Select NP_071332.2:p.Val354_Ala359del
Search 100 bp 5'
Search 100 bp 3'