Canonical Allele Identifier: CA525178030
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1394912938
gnomAD v2: 1-101005589-ACGCGGCGGCCGCTGCCGTTGC-A
gnomAD v4: 1-100540033-ACGCGGCGGCCGCTGCCGTTGC-A
MyVariant Identifiers: chr1:g.101005590_101005610del (hg19) chr1:g.100540034_100540054del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540037_100540057del , CM000663.2:g.100540037_100540057del GRCh38
NC_000001.10:g.101005593_101005613del , CM000663.1:g.101005593_101005613del GRCh37
NC_000001.9:g.100778181_100778201del NCBI36
NG_053134.1:g.6866_6886del

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1071_1091del MANE Select ENSP00000314223.4:p.Ala358_Ala364del
ENST00000315033.4:c.1071_1091del ENSP00000314223.4:p.Ala358_Ala364del
NM_022049.2:c.1071_1091del NP_071332.2:p.Ala358_Ala364del
NM_022049.3:c.1071_1091del MANE Select NP_071332.2:p.Ala358_Ala364del
Search 100 bp 5'
Search 100 bp 3'