Canonical Allele Identifier: CA1184191489
Gene: GPR88 HGNC NCBI

Linked Data

dbSNP Id: rs1651727389
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.100540068_100540069insA , CM000663.2:g.100540068_100540069insA GRCh38
NC_000001.10:g.101005624_101005625insA , CM000663.1:g.101005624_101005625insA GRCh37
NC_000001.9:g.100778212_100778213insA NCBI36
NG_053134.1:g.6897_6898insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000315033.5:c.1102_1103insA MANE Select ENSP00000314223.4:p.Pro368HisfsTer20
ENST00000315033.4:c.1102_1103insA ENSP00000314223.4:p.Pro368HisfsTer20
NM_022049.2:c.1102_1103insA NP_071332.2:p.Pro368HisfsTer20
NM_022049.3:c.1102_1103insA MANE Select NP_071332.2:p.Pro368HisfsTer20
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