Canonical Allele Identifier: CA2646776703
Gene: GPR88 HGNC NCBI

Linked Data

gnomAD v4: 1-100539566-G-GCTGCTGGCGCAGACAGCT
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100539573_100539590dup , CM000663.2:g.100539573_100539590dup GRCh38
NC_000001.10:g.101005129_101005146dup , CM000663.1:g.101005129_101005146dup GRCh37
NC_000001.9:g.100777717_100777734dup NCBI36
NG_053134.1:g.6402_6419dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.607_624dup MANE Select ENSP00000314223.4:p.Leu208_Leu209insAlaGlnThrAlaLeuLeu
ENST00000315033.4:c.607_624dup ENSP00000314223.4:p.Leu208_Leu209insAlaGlnThrAlaLeuLeu
NM_022049.2:c.607_624dup NP_071332.2:p.Leu208_Leu209insAlaGlnThrAlaLeuLeu
NM_022049.3:c.607_624dup MANE Select NP_071332.2:p.Leu208_Leu209insAlaGlnThrAlaLeuLeu
Search 100 bp 5'
Search 100 bp 3'