Canonical Allele Identifier: CA913046932
Gene: GPR88 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.101005114_101005131del (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539558_100539575del , CM000663.2:g.100539558_100539575del GRCh38
NC_000001.10:g.101005114_101005131del , CM000663.1:g.101005114_101005131del GRCh37
NC_000001.9:g.100777702_100777719del NCBI36
NG_053134.1:g.6387_6404del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.592_609del MANE Select ENSP00000314223.4:p.Ala198_Ala203del
ENST00000315033.4:c.592_609del ENSP00000314223.4:p.Ala198_Ala203del
NM_022049.2:c.592_609del NP_071332.2:p.Ala198_Ala203del
NM_022049.3:c.592_609del MANE Select NP_071332.2:p.Ala198_Ala203del
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